| 8650232 | CV126807 | single nucleotide variant | NM_173833.5(SCARA5):c.916+512T>C | Lung cancer [RCV000107294] | uncertain significance | 8 | 27921059 | 27921059 | Human | | name |
| 155902459 | CV2356463 | single nucleotide variant | NM_173833.6(SCARA5):c.8A>G (p.Asn3Ser) | not specified [RCV004199381] | uncertain significance | 8 | 27987608 | 27987608 | Human | | name |
| 156270554 | CV2276630 | single nucleotide variant | NM_173833.6(SCARA5):c.13G>A (p.Ala5Thr) | not specified [RCV004146111] | uncertain significance | 8 | 27987603 | 27987603 | Human | | name |
| 156169405 | CV2266748 | single nucleotide variant | NM_173833.6(SCARA5):c.31G>A (p.Val11Ile) | not specified [RCV004137576] | uncertain significance | 8 | 27987585 | 27987585 | Human | | name |
| 155917678 | CV2332861 | single nucleotide variant | NM_173833.6(SCARA5):c.71T>C (p.Phe24Ser) | not specified [RCV004192124] | uncertain significance | 8 | 27987545 | 27987545 | Human | | name |
| 329393743 | CV2472019 | single nucleotide variant | NM_173833.6(SCARA5):c.46A>G (p.Thr16Ala) | not specified [RCV004283168] | uncertain significance | 8 | 27987570 | 27987570 | Human | | name |
| 598196257 | CV3900294 | single nucleotide variant | NM_173833.6(SCARA5):c.34A>G (p.Ser12Gly) | not specified [RCV005267915] | uncertain significance | 8 | 27987582 | 27987582 | Human | | name |
| 8632967 | CV88182 | single nucleotide variant | NM_173833.5(SCARA5):c.318G>A (p.Arg106=) | Malignant melanoma [RCV000068274] | not provided | 8 | 27922169 | 27922169 | Human | | name |
| 155971820 | CV2238675 | single nucleotide variant | NM_173833.6(SCARA5):c.224G>T (p.Gly75Val) | not specified [RCV004107574] | uncertain significance | 8 | 27966431 | 27966431 | Human | | name |
| 156089707 | CV2241490 | single nucleotide variant | NM_173833.6(SCARA5):c.229T>C (p.Phe77Leu) | not specified [RCV004104397] | uncertain significance | 8 | 27966426 | 27966426 | Human | | name |
| 156125500 | CV2283638 | single nucleotide variant | NM_173833.6(SCARA5):c.287G>A (p.Arg96His) | not specified [RCV004142181] | uncertain significance | 8 | 27922200 | 27922200 | Human | | name |
| 156112172 | CV2353403 | single nucleotide variant | NM_173833.6(SCARA5):c.172C>G (p.Leu58Val) | not specified [RCV004205862] | uncertain significance | 8 | 27966483 | 27966483 | Human | | name |
| 155928374 | CV2363269 | single nucleotide variant | NM_173833.6(SCARA5):c.145T>C (p.Cys49Arg) | not specified [RCV004213825] | uncertain significance | 8 | 27966510 | 27966510 | Human | | name |
| 156225131 | CV2390487 | single nucleotide variant | NM_173833.6(SCARA5):c.128G>A (p.Arg43Gln) | not specified [RCV004239026] | uncertain significance | 8 | 27966527 | 27966527 | Human | | name |
| 405743153 | CV3317175 | single nucleotide variant | NM_173833.6(SCARA5):c.289A>C (p.Asn97His) | not specified [RCV004452696] | uncertain significance | 8 | 27922198 | 27922198 | Human | | name |
| 407514425 | CV3483879 | single nucleotide variant | NM_173833.6(SCARA5):c.131G>A (p.Arg44Gln) | not specified [RCV004674541] | uncertain significance | 8 | 27966524 | 27966524 | Human | | name |
| 407461228 | CV3483881 | single nucleotide variant | NM_173833.6(SCARA5):c.130C>T (p.Arg44Trp) | not specified [RCV004658657] | uncertain significance | 8 | 27966525 | 27966525 | Human | | name |
| 598196245 | CV3900292 | single nucleotide variant | NM_173833.6(SCARA5):c.205G>T (p.Val69Phe) | not specified [RCV005267913] | uncertain significance | 8 | 27966450 | 27966450 | Human | | name |
| 598196250 | CV3900293 | single nucleotide variant | NM_173833.6(SCARA5):c.104G>A (p.Cys35Tyr) | not specified [RCV005267914] | uncertain significance | 8 | 27987512 | 27987512 | Human | | name |
| 156030719 | CV2202524 | single nucleotide variant | NM_173833.6(SCARA5):c.365C>T (p.Thr122Met) | not specified [RCV004080819] | uncertain significance | 8 | 27922122 | 27922122 | Human | | name |
| 155982092 | CV2208659 | single nucleotide variant | NM_173833.6(SCARA5):c.566A>G (p.Gln189Arg) | not specified [RCV004091172] | uncertain significance | 8 | 27921921 | 27921921 | Human | | name |
| 155981311 | CV2244062 | single nucleotide variant | NM_173833.6(SCARA5):c.799G>A (p.Val267Ile) | not specified [RCV004108541] | uncertain significance | 8 | 27921688 | 27921688 | Human | | name |
| 156107462 | CV2254305 | single nucleotide variant | NM_173833.6(SCARA5):c.619G>A (p.Asp207Asn) | not specified [RCV004129969] | uncertain significance | 8 | 27921868 | 27921868 | Human | | name |
| 156153788 | CV2303857 | single nucleotide variant | NM_173833.6(SCARA5):c.371A>G (p.Gln124Arg) | not specified [RCV004168146] | uncertain significance | 8 | 27922116 | 27922116 | Human | | name |
| 156260054 | CV2305033 | single nucleotide variant | NM_173833.6(SCARA5):c.602G>A (p.Arg201His) | not specified [RCV004168920] | uncertain significance | 8 | 27921885 | 27921885 | Human | | name |
| 156108974 | CV2313892 | single nucleotide variant | NM_173833.6(SCARA5):c.418C>A (p.Leu140Met) | not specified [RCV004164203] | uncertain significance | 8 | 27922069 | 27922069 | Human | | name |
| 156064367 | CV2340755 | single nucleotide variant | NM_173833.6(SCARA5):c.487A>G (p.Thr163Ala) | not specified [RCV004188117] | uncertain significance | 8 | 27922000 | 27922000 | Human | | name |
| 155907749 | CV2389966 | single nucleotide variant | NM_173833.6(SCARA5):c.772G>A (p.Asp258Asn) | not specified [RCV004238217] | uncertain significance | 8 | 27921715 | 27921715 | Human | | name |
| 329399277 | CV2436543 | single nucleotide variant | NM_173833.6(SCARA5):c.473C>A (p.Ala158Glu) | not specified [RCV004253701] | uncertain significance | 8 | 27922014 | 27922014 | Human | | name |
| 329354551 | CV2448396 | single nucleotide variant | NM_173833.6(SCARA5):c.433G>A (p.Ala145Thr) | not specified [RCV004256681] | uncertain significance | 8 | 27922054 | 27922054 | Human | | name |
| 329395227 | CV2458223 | single nucleotide variant | NM_173833.6(SCARA5):c.746G>A (p.Arg249Gln) | not specified [RCV004265884] | likely benign | 8 | 27921741 | 27921741 | Human | | name |
| 329364160 | CV2460305 | single nucleotide variant | NM_173833.6(SCARA5):c.518G>A (p.Arg173His) | not specified [RCV004266846] | uncertain significance | 8 | 27921969 | 27921969 | Human | | name |
| 401756254 | CV2687054 | single nucleotide variant | NM_173833.6(SCARA5):c.443G>A (p.Arg148Gln) | not specified [RCV004304375] | uncertain significance | 8 | 27922044 | 27922044 | Human | | name |
| 401763486 | CV2703888 | single nucleotide variant | NM_173833.6(SCARA5):c.830T>C (p.Leu277Pro) | not specified [RCV004306747] | uncertain significance | 8 | 27921657 | 27921657 | Human | | name |
| 401778759 | CV2735489 | single nucleotide variant | NM_173833.6(SCARA5):c.778C>T (p.Arg260Cys) | not specified [RCV004331048] | uncertain significance | 8 | 27921709 | 27921709 | Human | | name |
| 405743164 | CV3317176 | single nucleotide variant | NM_173833.6(SCARA5):c.361C>A (p.Leu121Met) | not specified [RCV004452697] | uncertain significance | 8 | 27922126 | 27922126 | Human | | name |
| 405743174 | CV3317177 | single nucleotide variant | NM_173833.6(SCARA5):c.427G>A (p.Ala143Thr) | not specified [RCV004452698] | uncertain significance | 8 | 27922060 | 27922060 | Human | | name |
| 405743180 | CV3317178 | single nucleotide variant | NM_173833.6(SCARA5):c.567G>T (p.Gln189His) | not specified [RCV004452699] | uncertain significance | 8 | 27921920 | 27921920 | Human | | name |
| 405743186 | CV3317179 | single nucleotide variant | NM_173833.6(SCARA5):c.674G>A (p.Gly225Asp) | not specified [RCV004452700] | uncertain significance | 8 | 27921813 | 27921813 | Human | | name |
| 405743194 | CV3317180 | single nucleotide variant | NM_173833.6(SCARA5):c.788G>C (p.Arg263Pro) | not specified [RCV004452701] | uncertain significance | 8 | 27921699 | 27921699 | Human | | name |
| 405743203 | CV3317181 | single nucleotide variant | NM_173833.6(SCARA5):c.923C>T (p.Pro308Leu) | not specified [RCV004452702] | uncertain significance | 8 | 27909737 | 27909737 | Human | | name |
| 407461232 | CV3483882 | single nucleotide variant | NM_173833.6(SCARA5):c.433G>T (p.Ala145Ser) | not specified [RCV004658658] | uncertain significance | 8 | 27922054 | 27922054 | Human | | name |
| 407461236 | CV3483883 | single nucleotide variant | NM_173833.6(SCARA5):c.512G>A (p.Arg171Gln) | not specified [RCV004658659] | uncertain significance | 8 | 27921975 | 27921975 | Human | | name |
| 407461240 | CV3483885 | single nucleotide variant | NM_173833.6(SCARA5):c.553C>A (p.Leu185Ile) | not specified [RCV004658660] | uncertain significance | 8 | 27921934 | 27921934 | Human | | name |
| 407461251 | CV3483888 | single nucleotide variant | NM_173833.6(SCARA5):c.391G>A (p.Ala131Thr) | not specified [RCV004658663] | uncertain significance | 8 | 27922096 | 27922096 | Human | | name |
| 597690108 | CV3601684 | single nucleotide variant | NM_173833.6(SCARA5):c.664G>T (p.Asp222Tyr) | not specified [RCV004858778] | uncertain significance | 8 | 27921823 | 27921823 | Human | | name |
| 597690159 | CV3601690 | single nucleotide variant | NM_173833.6(SCARA5):c.317G>A (p.Arg106Gln) | not specified [RCV004858784] | uncertain significance | 8 | 27922170 | 27922170 | Human | | name |
| 597690168 | CV3601691 | single nucleotide variant | NM_173833.6(SCARA5):c.572A>G (p.Glu191Gly) | not specified [RCV004858785] | uncertain significance | 8 | 27921915 | 27921915 | Human | | name |
| 597690179 | CV3601692 | single nucleotide variant | NM_173833.6(SCARA5):c.359A>G (p.Asp120Gly) | not specified [RCV004858786] | uncertain significance | 8 | 27922128 | 27922128 | Human | | name |
| 597690189 | CV3601693 | single nucleotide variant | NM_173833.6(SCARA5):c.365C>A (p.Thr122Lys) | not specified [RCV004858787] | uncertain significance | 8 | 27922122 | 27922122 | Human | | name |
| 598196235 | CV3900290 | single nucleotide variant | NM_173833.6(SCARA5):c.316C>T (p.Arg106Trp) | not specified [RCV005267911] | uncertain significance | 8 | 27922171 | 27922171 | Human | | name |
| 598196240 | CV3900291 | single nucleotide variant | NM_173833.6(SCARA5):c.631C>T (p.Arg211Cys) | not specified [RCV005267912] | uncertain significance | 8 | 27921856 | 27921856 | Human | | name |
| 8632966 | CV88181 | single nucleotide variant | NM_173833.5(SCARA5):c.808G>A (p.Glu270Lys) | Malignant melanoma [RCV000068273] | not provided | 8 | 27921679 | 27921679 | Human | | name |
| 156385509 | CV2227947 | single nucleotide variant | NM_173833.6(SCARA5):c.1006G>A (p.Gly336Arg) | not specified [RCV004096200] | uncertain significance | 8 | 27907238 | 27907238 | Human | | name |
| 156082269 | CV2301152 | single nucleotide variant | NM_173833.6(SCARA5):c.1009G>A (p.Glu337Lys) | not specified [RCV004160064] | uncertain significance | 8 | 27907235 | 27907235 | Human | | name |
| 156155452 | CV2314298 | single nucleotide variant | NM_173833.6(SCARA5):c.1225T>C (p.Tyr409His) | not specified [RCV004166652] | uncertain significance | 8 | 27879695 | 27879695 | Human | | name |
| 329391434 | CV2452338 | single nucleotide variant | NM_173833.6(SCARA5):c.1147G>A (p.Asp383Asn) | not specified [RCV004272669] | uncertain significance | 8 | 27904784 | 27904784 | Human | | name |
| 329374085 | CV2452835 | single nucleotide variant | NM_173833.6(SCARA5):c.1082T>G (p.Met361Arg) | not specified [RCV004275364] | uncertain significance | 8 | 27907162 | 27907162 | Human | | name |
| 405743139 | CV3317173 | single nucleotide variant | NM_173833.6(SCARA5):c.1048G>A (p.Asp350Asn) | not specified [RCV004452694] | uncertain significance | 8 | 27907196 | 27907196 | Human | | name |
| 405743146 | CV3317174 | single nucleotide variant | NM_173833.6(SCARA5):c.1202C>T (p.Pro401Leu) | not specified [RCV004452695] | uncertain significance | 8 | 27879718 | 27879718 | Human | | name |
| 407514426 | CV3483880 | single nucleotide variant | NM_173833.6(SCARA5):c.1411C>T (p.Arg471Cys) | not specified [RCV004674542] | uncertain significance | 8 | 27872011 | 27872011 | Human | | name |
| 407461244 | CV3483886 | single nucleotide variant | NM_173833.6(SCARA5):c.1372G>A (p.Asp458Asn) | not specified [RCV004658661] | uncertain significance | 8 | 27872050 | 27872050 | Human | | name |
| 407461247 | CV3483887 | single nucleotide variant | NM_173833.6(SCARA5):c.1171A>G (p.Met391Val) | not specified [RCV004658662] | uncertain significance | 8 | 27879749 | 27879749 | Human | | name |
| 407461256 | CV3483889 | single nucleotide variant | NM_173833.6(SCARA5):c.1169C>T (p.Pro390Leu) | not specified [RCV004658664] | uncertain significance | 8 | 27879751 | 27879751 | Human | | name |
| 597690116 | CV3601685 | single nucleotide variant | NM_173833.6(SCARA5):c.1063G>T (p.Ala355Ser) | not specified [RCV004858779] | uncertain significance | 8 | 27907181 | 27907181 | Human | | name |
| 597690129 | CV3601686 | single nucleotide variant | NM_173833.6(SCARA5):c.1378G>A (p.Val460Ile) | not specified [RCV004858780] | uncertain significance | 8 | 27872044 | 27872044 | Human | | name |
| 597690140 | CV3601687 | single nucleotide variant | NM_173833.6(SCARA5):c.1483C>T (p.His495Tyr) | not specified [RCV004858781] | uncertain significance | 8 | 27871939 | 27871939 | Human | | name |
| 597690150 | CV3601689 | single nucleotide variant | NM_173833.6(SCARA5):c.1346G>A (p.Gly449Glu) | not specified [RCV004858783] | uncertain significance | 8 | 27879574 | 27879574 | Human | | name |
