| 156195216 | CV2400474 | single nucleotide variant | NM_018915.4(PCDHGA2):c.26A>G (p.His9Arg) | not specified [RCV004246676] | uncertain significance | 5 | 141338997 | 141338997 | Human | | name |
| 401756731 | CV2732064 | single nucleotide variant | NM_018915.4(PCDHGA2):c.16A>C (p.Lys6Gln) | not specified [RCV004330672] | uncertain significance | 5 | 141338987 | 141338987 | Human | | name |
| 405744378 | CV3368178 | single nucleotide variant | NM_018915.4(PCDHGA2):c.13C>A (p.Gln5Lys) | not specified [RCV004498245] | uncertain significance | 5 | 141338984 | 141338984 | Human | | name |
| 156169456 | CV2337368 | single nucleotide variant | NM_018915.4(PCDHGA2):c.40G>A (p.Val14Ile) | not specified [RCV004187814] | uncertain significance | 5 | 141339011 | 141339011 | Human | | name |
| 405744478 | CV3368190 | single nucleotide variant | NM_018915.4(PCDHGA2):c.41T>C (p.Val14Ala) | not specified [RCV004498257] | uncertain significance | 5 | 141339012 | 141339012 | Human | | name |
| 156207075 | CV2307854 | single nucleotide variant | NM_018915.4(PCDHGA2):c.203C>A (p.Ser68Tyr) | not specified [RCV004170314] | uncertain significance | 5 | 141339174 | 141339174 | Human | | name |
| 401915165 | CV2825331 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1737C>T (p.Pro579=) | not provided [RCV003428645] | likely benign | 5 | 141340708 | 141340708 | Human | | name |
| 597738078 | CV3575311 | single nucleotide variant | NM_018915.4(PCDHGA2):c.166C>A (p.Pro56Thr) | not specified [RCV004844040] | uncertain significance | 5 | 141339137 | 141339137 | Human | | name |
| 8657747 | CV81083 | single nucleotide variant | NM_018915.3(PCDHGA2):c.1377C>T (p.Thr459=) | Malignant melanoma [RCV000061161] | not provided | 5 | 141340348 | 141340348 | Human | | name |
| 156110010 | CV2261556 | single nucleotide variant | NM_018915.4(PCDHGA2):c.511G>C (p.Ala171Pro) | not specified [RCV004125892] | uncertain significance | 5 | 141339482 | 141339482 | Human | | name |
| 156158072 | CV2262452 | single nucleotide variant | NM_018915.4(PCDHGA2):c.653G>T (p.Gly218Val) | not specified [RCV004128891] | uncertain significance | 5 | 141339624 | 141339624 | Human | | name |
| 155920962 | CV2276225 | single nucleotide variant | NM_018915.4(PCDHGA2):c.793A>G (p.Thr265Ala) | not specified [RCV004142172] | uncertain significance | 5 | 141339764 | 141339764 | Human | | name |
| 156088650 | CV2290720 | single nucleotide variant | NM_018915.4(PCDHGA2):c.890C>A (p.Thr297Lys) | not specified [RCV004149241] | uncertain significance | 5 | 141339861 | 141339861 | Human | | name |
| 156067284 | CV2324059 | single nucleotide variant | NM_018915.4(PCDHGA2):c.684C>G (p.Ile228Met) | not specified [RCV004178355] | uncertain significance | 5 | 141339655 | 141339655 | Human | | name |
| 156181496 | CV2353084 | single nucleotide variant | NM_018915.4(PCDHGA2):c.631G>A (p.Val211Ile) | not specified [RCV004203566] | uncertain significance | 5 | 141339602 | 141339602 | Human | | name |
| 401771464 | CV2722837 | single nucleotide variant | NM_018915.4(PCDHGA2):c.508T>C (p.Tyr170His) | not specified [RCV004325253] | uncertain significance | 5 | 141339479 | 141339479 | Human | | name |
| 401717912 | CV2724967 | single nucleotide variant | NM_018915.4(PCDHGA2):c.425T>C (p.Ile142Thr) | not specified [RCV004319731] | uncertain significance | 5 | 141339396 | 141339396 | Human | | name |
| 407483169 | CV3463231 | single nucleotide variant | NM_018915.4(PCDHGA2):c.359A>G (p.Glu120Gly) | not specified [RCV004653247] | uncertain significance | 5 | 141339330 | 141339330 | Human | | name |
| 407484481 | CV3463235 | single nucleotide variant | NM_018915.4(PCDHGA2):c.394C>A (p.Arg132Ser) | not specified [RCV004659473] | uncertain significance | 5 | 141339365 | 141339365 | Human | | name |
| 597737903 | CV3575302 | single nucleotide variant | NM_018915.4(PCDHGA2):c.749G>A (p.Ser250Asn) | not specified [RCV004844031] | uncertain significance | 5 | 141339720 | 141339720 | Human | | name |
| 597738034 | CV3575303 | single nucleotide variant | NM_018915.4(PCDHGA2):c.842T>C (p.Leu281Pro) | not specified [RCV004844032] | uncertain significance | 5 | 141339813 | 141339813 | Human | | name |
| 597738056 | CV3575307 | single nucleotide variant | NM_018915.4(PCDHGA2):c.692A>G (p.Lys231Arg) | not specified [RCV004844036] | uncertain significance | 5 | 141339663 | 141339663 | Human | | name |
| 597738062 | CV3575308 | single nucleotide variant | NM_018915.4(PCDHGA2):c.773G>A (p.Gly258Asp) | not specified [RCV004844037] | likely benign | 5 | 141339744 | 141339744 | Human | | name |
| 597738073 | CV3575310 | single nucleotide variant | NM_018915.4(PCDHGA2):c.298G>T (p.Ala100Ser) | not specified [RCV004844039] | uncertain significance | 5 | 141339269 | 141339269 | Human | | name |
| 597738088 | CV3575313 | single nucleotide variant | NM_018915.4(PCDHGA2):c.361G>C (p.Val121Leu) | not specified [RCV004844042] | uncertain significance | 5 | 141339332 | 141339332 | Human | | name |
| 598270225 | CV3996266 | single nucleotide variant | NM_018915.4(PCDHGA2):c.856G>A (p.Gly286Arg) | not specified [RCV005388984] | uncertain significance | 5 | 141339827 | 141339827 | Human | | name |
| 598270688 | CV3996271 | single nucleotide variant | NM_018915.4(PCDHGA2):c.605G>C (p.Arg202Pro) | not specified [RCV005388989] | uncertain significance | 5 | 141339576 | 141339576 | Human | | name |
| 156172751 | CV2194288 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1156C>T (p.Leu386Phe) | not specified [RCV004079405] | uncertain significance | 5 | 141340127 | 141340127 | Human | | name |
| 156246891 | CV2196289 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2228T>C (p.Val743Ala) | not specified [RCV004073637] | uncertain significance | 5 | 141341199 | 141341199 | Human | | name |
| 156030494 | CV2202458 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1721G>T (p.Gly574Val) | not specified [RCV004080762] | uncertain significance | 5 | 141340692 | 141340692 | Human | | name |
| 155978557 | CV2215048 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2106C>G (p.Cys702Trp) | not specified [RCV004084817] | uncertain significance | 5 | 141341077 | 141341077 | Human | | name |
| 156386209 | CV2228144 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1360C>T (p.Arg454Cys) | not specified [RCV004096360] | uncertain significance | 5 | 141340331 | 141340331 | Human | | name |
| 155985641 | CV2233906 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1654G>A (p.Val552Met) | not specified [RCV004104259] | uncertain significance | 5 | 141340625 | 141340625 | Human | | name |
| 156077220 | CV2281644 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2048T>A (p.Ile683Lys) | EBV-positive nodal T- and NK-cell lymphoma [RCV004560073]|not specified [RCV004153936] | likely benign | 5 | 141341019 | 141341019 | Human | | name |
| 156263973 | CV2289761 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1901A>C (p.Asp634Ala) | not specified [RCV004150446] | uncertain significance | 5 | 141340872 | 141340872 | Human | | name |
| 156004171 | CV2290122 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2152C>T (p.Arg718Cys) | not specified [RCV004152793] | uncertain significance | 5 | 141341123 | 141341123 | Human | | name |
| 156298954 | CV2310675 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1552C>T (p.Arg518Cys) | not specified [RCV004157334] | uncertain significance | 5 | 141340523 | 141340523 | Human | | name |
| 156153417 | CV2328530 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2161A>G (p.Lys721Glu) | not specified [RCV004175900] | uncertain significance | 5 | 141341132 | 141341132 | Human | | name |
| 156190340 | CV2339568 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1572G>T (p.Gln524His) | not specified [RCV004194233] | uncertain significance | 5 | 141340543 | 141340543 | Human | | name |
| 156169360 | CV2345545 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2055C>G (p.Asn685Lys) | not specified [RCV004198305] | uncertain significance | 5 | 141341026 | 141341026 | Human | | name |
| 155904436 | CV2353869 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2023C>G (p.Leu675Val) | not specified [RCV004201869] | uncertain significance | 5 | 141340994 | 141340994 | Human | | name |
| 155956069 | CV2387210 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1003G>A (p.Val335Ile) | not specified [RCV004238311] | likely benign | 5 | 141339974 | 141339974 | Human | | name |
| 329374529 | CV2430930 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2044G>A (p.Ala682Thr) | not specified [RCV004248530] | uncertain significance | 5 | 141341015 | 141341015 | Human | | name |
| 329373711 | CV2447343 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1895T>G (p.Leu632Arg) | not specified [RCV004262622] | uncertain significance | 5 | 141340866 | 141340866 | Human | | name |
| 329355057 | CV2448995 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1024G>A (p.Asp342Asn) | not specified [RCV004264075] | uncertain significance | 5 | 141339995 | 141339995 | Human | | name |
| 329356707 | CV2460492 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1228C>T (p.Leu410Phe) | not specified [RCV004268783] | uncertain significance | 5 | 141340199 | 141340199 | Human | | name |
| 329396242 | CV2462454 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2011A>C (p.Ile671Leu) | not specified [RCV004276642] | uncertain significance | 5 | 141340982 | 141340982 | Human | | name |
| 329396497 | CV2462605 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1636G>A (p.Val546Ile) | not specified [RCV004278550] | uncertain significance | 5 | 141340607 | 141340607 | Human | | name |
| 401724515 | CV2677903 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1646G>A (p.Ser549Asn) | not specified [RCV004294393] | uncertain significance | 5 | 141340617 | 141340617 | Human | | name |
| 401752347 | CV2682789 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2191A>G (p.Ser731Gly) | not specified [RCV004281762] | likely benign | 5 | 141341162 | 141341162 | Human | | name |
| 401773126 | CV2709135 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1805C>T (p.Ala602Val) | not specified [RCV004314465] | uncertain significance | 5 | 141340776 | 141340776 | Human | | name |
| 401721648 | CV2710085 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1505C>G (p.Ser502Cys) | not specified [RCV004315144] | uncertain significance | 5 | 141340476 | 141340476 | Human | | name |
| 401884441 | CV2758949 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2008G>A (p.Asp670Asn) | not specified [RCV004342265] | uncertain significance | 5 | 141340979 | 141340979 | Human | | name |
| 401884260 | CV2761617 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1430A>G (p.His477Arg) | not specified [RCV004337242] | uncertain significance | 5 | 141340401 | 141340401 | Human | | name |
| 401893706 | CV2765417 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1511A>T (p.Tyr504Phe) | not specified [RCV004339916] | uncertain significance | 5 | 141340482 | 141340482 | Human | | name |
| 401887726 | CV2772115 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1138G>A (p.Ala380Thr) | not specified [RCV004344768] | uncertain significance | 5 | 141340109 | 141340109 | Human | | name |
| 401872562 | CV2779718 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2389C>G (p.Leu797Val) | not specified [RCV004351403] | uncertain significance | 5 | 141341360 | 141341360 | Human | | name |
| 401883130 | CV2785546 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1138G>T (p.Ala380Ser) | not specified [RCV004363066] | uncertain significance | 5 | 141340109 | 141340109 | Human | | name |
| 401915167 | CV2825332 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1783G>A (p.Asp595Asn) | not provided [RCV003428646] | likely benign | 5 | 141340754 | 141340754 | Human | | name |
| 401915170 | CV2825333 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1936A>G (p.Ile646Val) | not provided [RCV003428647] | likely benign | 5 | 141340907 | 141340907 | Human | | name |
| 405744355 | CV3368175 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1060A>G (p.Ser354Gly) | not specified [RCV004498242] | uncertain significance | 5 | 141340031 | 141340031 | Human | | name |
| 405744362 | CV3368176 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1216A>C (p.Thr406Pro) | not specified [RCV004498243] | uncertain significance | 5 | 141340187 | 141340187 | Human | | name |
| 405744372 | CV3368177 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1346C>T (p.Ala449Val) | not specified [RCV004498244] | uncertain significance | 5 | 141340317 | 141340317 | Human | | name |
| 405744397 | CV3368180 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1628G>A (p.Ser543Asn) | not specified [RCV004498247] | uncertain significance | 5 | 141340599 | 141340599 | Human | | name |
| 405744406 | CV3368181 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1654G>C (p.Val552Leu) | not specified [RCV004498248] | uncertain significance | 5 | 141340625 | 141340625 | Human | | name |
| 405744412 | CV3368182 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1880G>A (p.Arg627His) | not specified [RCV004498249] | uncertain significance | 5 | 141340851 | 141340851 | Human | | name |
| 405744419 | CV3368183 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1976C>T (p.Thr659Met) | not specified [RCV004498250] | uncertain significance | 5 | 141340947 | 141340947 | Human | | name |
| 405744424 | CV3368184 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2026G>A (p.Gly676Ser) | not specified [RCV004498251] | uncertain significance | 5 | 141340997 | 141340997 | Human | | name |
| 405744443 | CV3368186 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2090T>C (p.Val697Ala) | not specified [RCV004498253] | uncertain significance | 5 | 141341061 | 141341061 | Human | | name |
| 405744470 | CV3368189 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2404A>G (p.Arg802Gly) | not specified [RCV004498256] | likely benign | 5 | 141341375 | 141341375 | Human | | name |
| 407484468 | CV3463232 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1381A>G (p.Ile461Val) | not specified [RCV004659471] | uncertain significance | 5 | 141340352 | 141340352 | Human | | name |
| 407484475 | CV3463233 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2258A>G (p.Tyr753Cys) | not specified [RCV004659472] | uncertain significance | 5 | 141341229 | 141341229 | Human | | name |
| 407483176 | CV3463234 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1683G>T (p.Glu561Asp) | not specified [RCV004653248] | uncertain significance | 5 | 141340654 | 141340654 | Human | | name |
| 407484843 | CV3463236 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1591T>C (p.Trp531Arg) | not specified [RCV004659474] | uncertain significance | 5 | 141340562 | 141340562 | Human | | name |
| 407483183 | CV3463237 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1444A>G (p.Asn482Asp) | not specified [RCV004653249] | likely benign | 5 | 141340415 | 141340415 | Human | | name |
| 597738039 | CV3575304 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1255A>G (p.Asn419Asp) | not specified [RCV004844033] | uncertain significance | 5 | 141340226 | 141340226 | Human | | name |
| 597738046 | CV3575305 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1841C>A (p.Pro614Gln) | not specified [RCV004844034] | uncertain significance | 5 | 141340812 | 141340812 | Human | | name |
| 597738051 | CV3575306 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1836C>A (p.Ser612Arg) | not specified [RCV004844035] | uncertain significance | 5 | 141340807 | 141340807 | Human | | name |
| 597738067 | CV3575309 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1738C>G (p.Arg580Gly) | not specified [RCV004844038] | uncertain significance | 5 | 141340709 | 141340709 | Human | | name |
| 597738083 | CV3575312 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1674C>A (p.Asn558Lys) | not specified [RCV004844041] | uncertain significance | 5 | 141340645 | 141340645 | Human | | name |
| 597738093 | CV3575314 | single nucleotide variant | NM_018915.4(PCDHGA2):c.2247C>G (p.Phe749Leu) | not specified [RCV004844043] | uncertain significance | 5 | 141341218 | 141341218 | Human | | name |
| 598195643 | CV3996265 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1879C>A (p.Arg627Ser) | not specified [RCV005397566] | uncertain significance | 5 | 141340850 | 141340850 | Human | | name |
| 598270230 | CV3996267 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1288C>A (p.Pro430Thr) | not specified [RCV005388985] | uncertain significance | 5 | 141340259 | 141340259 | Human | | name |
| 598270235 | CV3996268 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1395C>A (p.Asn465Lys) | not specified [RCV005388986] | uncertain significance | 5 | 141340366 | 141340366 | Human | | name |
| 598270240 | CV3996269 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1405G>T (p.Ala469Ser) | not specified [RCV005388987] | uncertain significance | 5 | 141340376 | 141340376 | Human | | name |
| 598270683 | CV3996272 | single nucleotide variant | NM_018915.4(PCDHGA2):c.1166A>T (p.Asp389Val) | not specified [RCV005388990] | uncertain significance | 5 | 141340137 | 141340137 | Human | | name |
| 8657748 | CV81084 | single nucleotide variant | NM_018915.3(PCDHGA2):c.1384C>T (p.Pro462Ser) | Malignant melanoma [RCV000061162] | not provided | 5 | 141340355 | 141340355 | Human | | name |
| 8658680 | CV86641 | single nucleotide variant | NM_018915.3(PCDHGA2):c.1031C>T (p.Ala344Val) | Malignant melanoma [RCV000066732] | not provided | 5 | 141340002 | 141340002 | Human | | name |
| 8657776 | CV86642 | single nucleotide variant | NM_018915.3(PCDHGA2):c.1793C>T (p.Ser598Leu) | Malignant melanoma [RCV000066733] | not provided | 5 | 141340764 | 141340764 | Human | | name |
| 8657777 | CV86643 | single nucleotide variant | NM_018915.3(PCDHGA2):c.2273C>T (p.Ser758Phe) | Malignant melanoma [RCV000066734] | not provided | 5 | 141341244 | 141341244 | Human | | name |
