| 155964981 | CV2395903 | single nucleotide variant | NM_018929.3(PCDHGC5):c.95G>A (p.Arg32His) | not specified [RCV004237461] | uncertain significance | 5 | 141489335 | 141489335 | Human | | name |
| 329397199 | CV2456683 | single nucleotide variant | NM_018929.3(PCDHGC5):c.31G>A (p.Gly11Arg) | not specified [RCV004277859] | uncertain significance | 5 | 141489271 | 141489271 | Human | | name |
| 598195855 | CV3996450 | single nucleotide variant | NM_018929.3(PCDHGC5):c.74G>C (p.Gly25Ala) | not specified [RCV005397598] | uncertain significance | 5 | 141489314 | 141489314 | Human | | name |
| 156059438 | CV2383539 | single nucleotide variant | NM_018929.3(PCDHGC5):c.218G>A (p.Arg73His) | not specified [RCV004222544] | likely benign | 5 | 141489458 | 141489458 | Human | | name |
| 597739091 | CV3571671 | single nucleotide variant | NM_018929.3(PCDHGC5):c.238A>G (p.Met80Val) | not specified [RCV004844237] | likely benign | 5 | 141489478 | 141489478 | Human | | name |
| 598271280 | CV3996451 | single nucleotide variant | NM_018929.3(PCDHGC5):c.185G>A (p.Arg62Gln) | not specified [RCV005389137] | uncertain significance | 5 | 141489425 | 141489425 | Human | | name |
| 15196901 | CV698875 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1173G>A (p.Pro391=) | not provided [RCV000956314] | benign | 5 | 141490413 | 141490413 | Human | | name |
| 15196904 | CV698876 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1407G>A (p.Pro469=) | not provided [RCV000956315] | benign | 5 | 141490647 | 141490647 | Human | | name |
| 15196908 | CV698877 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2013T>C (p.Pro671=) | not provided [RCV000956316] | benign | 5 | 141491253 | 141491253 | Human | | name |
| 15184314 | CV709680 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1965A>G (p.Ser655=) | not provided [RCV000975083] | benign | 5 | 141491205 | 141491205 | Human | | name |
| 15162666 | CV734882 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2121C>A (p.Val707=) | not provided [RCV000903600] | benign | 5 | 141491361 | 141491361 | Human | | name |
| 156065436 | CV2196927 | single nucleotide variant | NM_018929.3(PCDHGC5):c.353G>A (p.Arg118His) | not specified [RCV004071389] | uncertain significance | 5 | 141489593 | 141489593 | Human | | name |
| 156333161 | CV2214551 | single nucleotide variant | NM_018929.3(PCDHGC5):c.707A>G (p.Asn236Ser) | not specified [RCV004088599] | uncertain significance | 5 | 141489947 | 141489947 | Human | | name |
| 155905674 | CV2303161 | single nucleotide variant | NM_018929.3(PCDHGC5):c.684C>G (p.Ile228Met) | not specified [RCV004156927] | uncertain significance | 5 | 141489924 | 141489924 | Human | | name |
| 155912023 | CV2308600 | single nucleotide variant | NM_018929.3(PCDHGC5):c.967C>T (p.Arg323Cys) | not specified [RCV004167159] | uncertain significance | 5 | 141490207 | 141490207 | Human | | name |
| 156068549 | CV2345994 | single nucleotide variant | NM_018929.3(PCDHGC5):c.941G>A (p.Arg314His) | not specified [RCV004199026] | uncertain significance | 5 | 141490181 | 141490181 | Human | | name |
| 155919379 | CV2360250 | single nucleotide variant | NM_018929.3(PCDHGC5):c.967C>G (p.Arg323Gly) | not specified [RCV004208596] | uncertain significance | 5 | 141490207 | 141490207 | Human | | name |
| 156258193 | CV2366034 | single nucleotide variant | NM_018929.3(PCDHGC5):c.968G>A (p.Arg323His) | not specified [RCV004208033] | uncertain significance | 5 | 141490208 | 141490208 | Human | | name |
| 156105980 | CV2387050 | single nucleotide variant | NM_018929.3(PCDHGC5):c.421C>T (p.Arg141Cys) | not specified [RCV004226795] | uncertain significance | 5 | 141489661 | 141489661 | Human | | name |
| 156268088 | CV2398402 | single nucleotide variant | NM_018929.3(PCDHGC5):c.890C>A (p.Pro297His) | not specified [RCV004237735] | uncertain significance | 5 | 141490130 | 141490130 | Human | | name |
| 401865234 | CV2791569 | single nucleotide variant | NM_018929.3(PCDHGC5):c.729A>T (p.Gln243His) | not specified [RCV004358941] | uncertain significance | 5 | 141489969 | 141489969 | Human | | name |
| 405760544 | CV3364545 | single nucleotide variant | NM_018929.3(PCDHGC5):c.317T>C (p.Val106Ala) | not specified [RCV004500560] | uncertain significance | 5 | 141489557 | 141489557 | Human | | name |
| 405760554 | CV3364546 | single nucleotide variant | NM_018929.3(PCDHGC5):c.352C>T (p.Arg118Cys) | not specified [RCV004500561] | uncertain significance | 5 | 141489592 | 141489592 | Human | | name |
| 405760561 | CV3364547 | single nucleotide variant | NM_018929.3(PCDHGC5):c.422G>C (p.Arg141Pro) | not specified [RCV004500562] | uncertain significance | 5 | 141489662 | 141489662 | Human | | name |
| 405760568 | CV3364548 | single nucleotide variant | NM_018929.3(PCDHGC5):c.479C>T (p.Pro160Leu) | not specified [RCV004500563] | uncertain significance | 5 | 141489719 | 141489719 | Human | | name |
| 405760575 | CV3364549 | single nucleotide variant | NM_018929.3(PCDHGC5):c.493A>C (p.Asn165His) | not specified [RCV004500564] | uncertain significance | 5 | 141489733 | 141489733 | Human | | name |
| 405760587 | CV3364550 | single nucleotide variant | NM_018929.3(PCDHGC5):c.520C>T (p.Pro174Ser) | not specified [RCV004500565] | uncertain significance | 5 | 141489760 | 141489760 | Human | | name |
| 405760595 | CV3364551 | single nucleotide variant | NM_018929.3(PCDHGC5):c.551C>T (p.Thr184Ile) | not specified [RCV004500566] | uncertain significance | 5 | 141489791 | 141489791 | Human | | name |
| 405760607 | CV3364553 | single nucleotide variant | NM_018929.3(PCDHGC5):c.665G>A (p.Arg222His) | not specified [RCV004500568] | likely benign | 5 | 141489905 | 141489905 | Human | | name |
| 407483698 | CV3459871 | single nucleotide variant | NM_018929.3(PCDHGC5):c.910G>A (p.Val304Met) | not specified [RCV004653317] | uncertain significance | 5 | 141490150 | 141490150 | Human | | name |
| 597739116 | CV3571675 | single nucleotide variant | NM_018929.3(PCDHGC5):c.754C>A (p.Pro252Thr) | not specified [RCV004844241] | uncertain significance | 5 | 141489994 | 141489994 | Human | | name |
| 598271266 | CV3996447 | single nucleotide variant | NM_018929.3(PCDHGC5):c.638C>T (p.Thr213Ile) | not specified [RCV005389135] | uncertain significance | 5 | 141489878 | 141489878 | Human | | name |
| 156246983 | CV2202796 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2304C>G (p.Asp768Glu) | not specified [RCV004073658] | uncertain significance | 5 | 141491544 | 141491544 | Human | | name |
| 156178027 | CV2229237 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1714G>A (p.Glu572Lys) | not specified [RCV004101050] | uncertain significance | 5 | 141490954 | 141490954 | Human | | name |
| 156071163 | CV2254823 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2392C>A (p.Pro798Thr) | not specified [RCV004115286] | uncertain significance | 5 | 141491632 | 141491632 | Human | | name |
| 156339134 | CV2271374 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1585A>T (p.Met529Leu) | not specified [RCV004136486] | uncertain significance | 5 | 141490825 | 141490825 | Human | | name |
| 156018795 | CV2272387 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1843G>A (p.Ala615Thr) | not specified [RCV004133311] | uncertain significance | 5 | 141491083 | 141491083 | Human | | name |
| 156061098 | CV2280334 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2351G>A (p.Gly784Asp) | not specified [RCV004140527] | uncertain significance | 5 | 141491591 | 141491591 | Human | | name |
| 155959468 | CV2285278 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1531C>T (p.Pro511Ser) | not specified [RCV004137374] | uncertain significance | 5 | 141490771 | 141490771 | Human | | name |
| 156260389 | CV2305086 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1153G>A (p.Val385Met) | not specified [RCV004168963] | uncertain significance | 5 | 141490393 | 141490393 | Human | | name |
| 156207968 | CV2360492 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2084T>C (p.Ile695Thr) | not specified [RCV004210857] | uncertain significance | 5 | 141491324 | 141491324 | Human | | name |
| 156168111 | CV2373762 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1130G>A (p.Arg377Gln) | not specified [RCV004224705] | uncertain significance | 5 | 141490370 | 141490370 | Human | | name |
| 156207185 | CV2382325 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1129C>T (p.Arg377Trp) | not specified [RCV004230672] | uncertain significance | 5 | 141490369 | 141490369 | Human | | name |
| 329400636 | CV2438595 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1634A>G (p.His545Arg) | not specified [RCV004261769] | uncertain significance | 5 | 141490874 | 141490874 | Human | | name |
| 329394211 | CV2450181 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2300C>A (p.Thr767Lys) | not specified [RCV004270999] | uncertain significance | 5 | 141491540 | 141491540 | Human | | name |
| 329358481 | CV2450330 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1406C>G (p.Pro469Arg) | not specified [RCV004271413] | uncertain significance | 5 | 141490646 | 141490646 | Human | | name |
| 329380331 | CV2466562 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2030C>G (p.Ser677Cys) | not specified [RCV004274098] | uncertain significance | 5 | 141491270 | 141491270 | Human | | name |
| 329353399 | CV2469213 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2170G>T (p.Asp724Tyr) | not specified [RCV004280562] | uncertain significance | 5 | 141491410 | 141491410 | Human | | name |
| 329398537 | CV2471594 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2443C>G (p.Leu815Val) | not specified [RCV004286892] | uncertain significance | 5 | 141491683 | 141491683 | Human | | name |
| 401780228 | CV2673927 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1886G>A (p.Arg629His) | not specified [RCV004293301] | uncertain significance | 5 | 141491126 | 141491126 | Human | | name |
| 401754293 | CV2717329 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1610G>A (p.Arg537Gln) | not specified [RCV004330206] | uncertain significance | 5 | 141490850 | 141490850 | Human | | name |
| 401887269 | CV2773280 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2014G>A (p.Glu672Lys) | not specified [RCV004353949] | uncertain significance | 5 | 141491254 | 141491254 | Human | | name |
| 401858431 | CV2774186 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2426G>A (p.Arg809Gln) | not specified [RCV004345773] | uncertain significance | 5 | 141491666 | 141491666 | Human | | name |
| 401876490 | CV2782938 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1202A>T (p.Glu401Val) | not specified [RCV004361734] | uncertain significance | 5 | 141490442 | 141490442 | Human | | name |
| 405760531 | CV3364543 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1717C>G (p.His573Asp) | not specified [RCV004500558] | uncertain significance | 5 | 141490957 | 141490957 | Human | | name |
| 407483709 | CV3459873 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1130G>C (p.Arg377Pro) | not specified [RCV004653318] | uncertain significance | 5 | 141490370 | 141490370 | Human | | name |
| 407483719 | CV3459874 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2201A>G (p.Gln734Arg) | not specified [RCV004653319] | uncertain significance | 5 | 141491441 | 141491441 | Human | | name |
| 407483729 | CV3459875 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1309C>T (p.His437Tyr) | not specified [RCV004653320] | uncertain significance | 5 | 141490549 | 141490549 | Human | | name |
| 407483736 | CV3459876 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1469C>T (p.Thr490Ile) | not specified [RCV004653321] | uncertain significance | 5 | 141490709 | 141490709 | Human | | name |
| 597739086 | CV3571670 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1172C>A (p.Pro391Gln) | not specified [RCV004844236] | uncertain significance | 5 | 141490412 | 141490412 | Human | | name |
| 597739098 | CV3571672 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1124G>A (p.Arg375Gln) | not specified [RCV004844238] | uncertain significance | 5 | 141490364 | 141490364 | Human | | name |
| 597739104 | CV3571673 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1750C>T (p.Pro584Ser) | not specified [RCV004844239] | uncertain significance | 5 | 141490990 | 141490990 | Human | | name |
| 597739111 | CV3571674 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2309A>T (p.Gln770Leu) | not specified [RCV004844240] | uncertain significance | 5 | 141491549 | 141491549 | Human | | name |
| 598271254 | CV3996445 | single nucleotide variant | NM_018929.3(PCDHGC5):c.1618G>C (p.Gly540Arg) | not specified [RCV005389133] | uncertain significance | 5 | 141490858 | 141490858 | Human | | name |
| 598271259 | CV3996446 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2453G>A (p.Arg818Gln) | not specified [RCV005389134] | uncertain significance | 5 | 141491693 | 141491693 | Human | | name |
| 598271272 | CV3996448 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2087T>C (p.Val696Ala) | not specified [RCV005389136] | uncertain significance | 5 | 141491327 | 141491327 | Human | | name |
| 598195848 | CV3996449 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2177G>T (p.Gly726Val) | not specified [RCV005397597] | uncertain significance | 5 | 141491417 | 141491417 | Human | | name |
| 598271287 | CV3996452 | single nucleotide variant | NM_018929.3(PCDHGC5):c.2251G>C (p.Val751Leu) | not specified [RCV005389138] | uncertain significance | 5 | 141491491 | 141491491 | Human | | name |
| 8657789 | CV86658 | single nucleotide variant | NM_018929.2(PCDHGC5):c.2080C>T (p.Leu694Phe) | Malignant melanoma [RCV000066749] | not provided | 5 | 141491320 | 141491320 | Human | | name |
