| 14 | g.74259640G>A | CA7266401 | VSX2 | c.618G>A (p.Arg206=)
| ClinVar dbSNP ExAC gnomAD v2 |
| 14 | g.74259640G>C | CA487155837 | VSX2 | c.618G>C (p.Arg206=)
| |
| 14 | g.74259640G= | CA2146964470 | VSX2 | c.618G= (p.Arg206=)
| |
| 14 | g.74259640G>T | CA487155836 | VSX2 | c.618G>T (p.Arg206=)
| |
| 14 | g.74259641G>A | CA390369202 | VSX2 | c.619G>A (p.Glu207Lys)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259641G>C | CA390369203 | VSX2 | c.619G>C (p.Glu207Gln)
| |
| 14 | g.74259641G= | CA2146964471 | VSX2 | c.619G= (p.Glu207=)
| |
| 14 | g.74259641G>T | CA390369204 | VSX2 | c.619G>T (p.Glu207Ter)
| gnomAD v4 |
| 14 | g.74259642A= | CA2146964472 | VSX2 | c.620A= (p.Glu207=)
| |
| 14 | g.74259642A>C | CA390369205 | VSX2 | c.620A>C (p.Glu207Ala)
| |
| 14 | g.74259642A>G | CA390369206 | VSX2 | c.620A>G (p.Glu207Gly)
| |
| 14 | g.74259642A>T | CA390369207 | VSX2 | c.620A>T (p.Glu207Val)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259643G>A | CA487155839 | VSX2 | c.621G>A (p.Glu207=)
| gnomAD v4 |
| 14 | g.74259643G>C | CA390369208 | VSX2 | c.621G>C (p.Glu207Asp)
| |
| 14 | g.74259643G>T | CA390369209 | VSX2 | c.621G>T (p.Glu207Asp)
| |
| 14 | g.74259644A>C | CA390369212 | VSX2 | c.622A>C (p.Lys208Gln)
| |
| 14 | g.74259644A>G | CA390369211 | VSX2 | c.622A>G (p.Lys208Glu)
| |
| 14 | g.74259644A>T | CA390369210 | VSX2 | c.622A>T (p.Lys208Ter)
| |
| 14 | g.74259645A= | CA2146964473 | VSX2 | c.623A= (p.Lys208=)
| |
| 14 | g.74259645A>C | CA390369213 | VSX2 | c.623A>C (p.Lys208Thr)
| |
| 14 | g.74259645A>G | CA390369215 | VSX2 | c.623A>G (p.Lys208Arg)
| |
| 14 | g.74259645A>T | CA390369214 | VSX2 | c.623A>T (p.Lys208Met)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259646G>A | CA487155844 | VSX2 | c.624G>A (p.Lys208=)
| gnomAD v4 |
| 14 | g.74259646G>C | CA390369216 | VSX2 | c.624G>C (p.Lys208Asn)
| |
| 14 | g.74259646G>T | CA390369217 | VSX2 | c.624G>T (p.Lys208Asn)
| |
| 14 | g.74259647T>A | CA390369218 | VSX2 | c.625T>A (p.Cys209Ser)
| |
| 14 | g.74259647T>C | CA390369219 | VSX2 | c.625T>C (p.Cys209Arg)
| gnomAD v4 |
| 14 | g.74259647T>G | CA7266402 | VSX2 | c.625T>G (p.Cys209Gly)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259647T= | CA2146964474 | VSX2 | c.625T= (p.Cys209=)
| |
| 14 | g.74259648G>A | CA390369220 | VSX2 | c.626G>A (p.Cys209Tyr)
| |
| 14 | g.74259648G>C | CA390369221 | VSX2 | c.626G>C (p.Cys209Ser)
| dbSNP |
| 14 | g.74259648G= | CA2146964475 | VSX2 | c.626G= (p.Cys209=)
| |
| 14 | g.74259648G>T | CA390369222 | VSX2 | c.626G>T (p.Cys209Phe)
| |
| 14 | g.74259649C>A | CA390369223 | VSX2 | c.627C>A (p.Cys209Ter)
| |
| 14 | g.74259649C>G | CA390369224 | VSX2 | c.627C>G (p.Cys209Trp)
| |
| 14 | g.74259649C>T | CA487155846 | VSX2 | c.627C>T (p.Cys209=)
| ClinVar |
| 14 | g.74259650T>A | CA390369225 | VSX2 | c.628T>A (p.Trp210Arg)
| |
| 14 | g.74259650T>C | CA390369226 | VSX2 | c.628T>C (p.Trp210Arg)
| |
| 14 | g.74259650T>G | CA390369227 | VSX2 | c.628T>G (p.Trp210Gly)
| |
| 14 | g.74259651G>A | CA390369230 | VSX2 | c.629G>A (p.Trp210Ter)
| |
| 14 | g.74259651G>C | CA390369228 | VSX2 | c.629G>C (p.Trp210Ser)
| gnomAD v4 |
| 14 | g.74259651G>T | CA390369229 | VSX2 | c.629G>T (p.Trp210Leu)
| |
| 14 | g.74259652G>A | CA390369231 | VSX2 | c.630G>A (p.Trp210Ter)
| COSMIC |
| 14 | g.74259652G>C | CA390369232 | VSX2 | c.630G>C (p.Trp210Cys)
| |
| 14 | g.74259652G>T | CA390369233 | VSX2 | c.630G>T (p.Trp210Cys)
| |
| 14 | g.74259653G>A | CA390369234 | VSX2 | c.631G>A (p.Gly211Ser)
| |
| 14 | g.74259653G>C | CA390369235 | VSX2 | c.631G>C (p.Gly211Arg)
| |
| 14 | g.74259653G>T | CA390369236 | VSX2 | c.631G>T (p.Gly211Cys)
| |
| 14 | g.74259654G>A | CA390369237 | VSX2 | c.632G>A (p.Gly211Asp)
| gnomAD v4 |
| 14 | g.74259654G>C | CA390369238 | VSX2 | c.632G>C (p.Gly211Ala)
| |
| 14 | g.74259654G>T | CA390369239 | VSX2 | c.632G>T (p.Gly211Val)
| |
| 14 | g.74259655C>A | CA487155848 | VSX2 | c.633C>A (p.Gly211=)
| |
| 14 | g.74259655C>G | CA487155851 | VSX2 | c.633C>G (p.Gly211=)
| |
| 14 | g.74259655C>T | CA487155849 | VSX2 | c.633C>T (p.Gly211=)
| |
| 14 | g.74259656del | CA2695219547 | VSX2 | c.634del (p.Arg212GlyfsTer?)
| ClinVar |
| 14 | g.74259656C>A | CA487155852 | VSX2 | c.634C>A (p.Arg212=)
| dbSNP |
| 14 | g.74259656C= | CA2146964476 | VSX2 | c.634C= (p.Arg212=)
| |
| 14 | g.74259656C>G | CA390369240 | VSX2 | c.634C>G (p.Arg212Gly)
| |
| 14 | g.74259656C>T | CA263556562 | VSX2 | c.634C>T (p.Arg212Trp)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259657G>A | CA390369241 | VSX2 | c.635G>A (p.Arg212Gln)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.74259657G>C | CA390369242 | VSX2 | c.635G>C (p.Arg212Pro)
| gnomAD v4 |
| 14 | g.74259657G= | CA2146964477 | VSX2 | c.635G= (p.Arg212=)
| |
| 14 | g.74259657G>T | CA7266403 | VSX2 | c.635G>T (p.Arg212Leu)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.74259658G>A | CA487155854 | VSX2 | c.636G>A (p.Arg212=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259658G>C | CA487155855 | VSX2 | c.636G>C (p.Arg212=)
| |
| 14 | g.74259658G= | CA2146964478 | VSX2 | c.636G= (p.Arg212=)
| |
| 14 | g.74259658G>T | CA487155856 | VSX2 | c.636G>T (p.Arg212=)
| |
| 14 | g.74259659A>C | CA390369243 | VSX2 | c.637A>C (p.Ser213Arg)
| |
| 14 | g.74259659A>G | CA390369244 | VSX2 | c.637A>G (p.Ser213Gly)
| |
| 14 | g.74259659A>T | CA390369245 | VSX2 | c.637A>T (p.Ser213Cys)
| |
| 14 | g.74259660G>A | CA390369246 | VSX2 | c.638G>A (p.Ser213Asn)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259660G>C | CA390369247 | VSX2 | c.638G>C (p.Ser213Thr)
| |
| 14 | g.74259660G= | CA2146964479 | VSX2 | c.638G= (p.Ser213=)
| |
| 14 | g.74259660G>T | CA390369248 | VSX2 | c.638G>T (p.Ser213Ile)
| |
| 14 | g.74259661C>A | CA390369249 | VSX2 | c.639C>A (p.Ser213Arg)
| |
| 14 | g.74259661C>G | CA390369250 | VSX2 | c.639C>G (p.Ser213Arg)
| |
| 14 | g.74259661C>T | CA487155857 | VSX2 | c.639C>T (p.Ser213=)
| |
| 14 | g.74259662A>C | CA390369251 | VSX2 | c.640A>C (p.Ser214Arg)
| |
| 14 | g.74259662A>G | CA390369252 | VSX2 | c.640A>G (p.Ser214Gly)
| gnomAD v4 |
| 14 | g.74259662A>T | CA390369253 | VSX2 | c.640A>T (p.Ser214Cys)
| |
| 14 | g.74259663G>A | CA390369254 | VSX2 | c.641G>A (p.Ser214Asn)
| |
| 14 | g.74259663G>C | CA390369255 | VSX2 | c.641G>C (p.Ser214Thr)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259663G= | CA2146964480 | VSX2 | c.641G= (p.Ser214=)
| |
| 14 | g.74259663G>T | CA390369256 | VSX2 | c.641G>T (p.Ser214Ile)
| |
| 14 | g.74259665_74259666del | CA2625651043 | VSX2 | c.643_644del (p.Val215HisfsTer?)
| gnomAD v4 |
| 14 | g.74259664T>A | CA390369257 | VSX2 | c.642T>A (p.Ser214Arg)
| |
| 14 | g.74259664T>C | CA487155859 | VSX2 | c.642T>C (p.Ser214=)
| ClinVar gnomAD v4 |
| 14 | g.74259664T>G | CA390369258 | VSX2 | c.642T>G (p.Ser214Arg)
| |
| 14 | g.74259665G>A | CA390369259 | VSX2 | c.643G>A (p.Val215Ile)
| |
| 14 | g.74259665G>C | CA390369260 | VSX2 | c.643G>C (p.Val215Leu)
| |
| 14 | g.74259665G>T | CA390369261 | VSX2 | c.643G>T (p.Val215Phe)
| |
| 14 | g.74259666T>A | CA390369262 | VSX2 | c.644T>A (p.Val215Asp)
| |
| 14 | g.74259666T>C | CA390369263 | VSX2 | c.644T>C (p.Val215Ala)
| |
| 14 | g.74259666T>G | CA390369264 | VSX2 | c.644T>G (p.Val215Gly)
| |
| 14 | g.74259667C>A | CA487155863 | VSX2 | c.645C>A (p.Val215=)
| |
| 14 | g.74259667C>G | CA487155864 | VSX2 | c.645C>G (p.Val215=)
| |
| 14 | g.74259667C>T | CA487155865 | VSX2 | c.645C>T (p.Val215=)
| |
| 14 | g.74259668A>C | CA390369265 | VSX2 | c.646A>C (p.Met216Leu)
| |
| 14 | g.74259668A>G | CA390369266 | VSX2 | c.646A>G (p.Met216Val)
| |
| 14 | g.74259668A>T | CA390369267 | VSX2 | c.646A>T (p.Met216Leu)
| |
| 14 | g.74259669T>A | CA390369268 | VSX2 | c.647T>A (p.Met216Lys)
| |
| 14 | g.74259669T>C | CA390369269 | VSX2 | c.647T>C (p.Met216Thr)
| dbSNP |
| 14 | g.74259669T>G | CA390369270 | VSX2 | c.647T>G (p.Met216Arg)
| |
| 14 | g.74259669T= | CA2146964481 | VSX2 | c.647T= (p.Met216=)
| |
| 14 | g.74259670G>A | CA390369273 | VSX2 | c.648G>A (p.Met216Ile)
| |
| 14 | g.74259670G>C | CA390369272 | VSX2 | c.648G>C (p.Met216Ile)
| |
| 14 | g.74259670G>T | CA390369271 | VSX2 | c.648G>T (p.Met216Ile)
| |
| 14 | g.74259671G>A | CA390369274 | VSX2 | c.649G>A (p.Ala217Thr)
| COSMIC |
| 14 | g.74259671G>C | CA390369275 | VSX2 | c.649G>C (p.Ala217Pro)
| ClinVar dbSNP |
| 14 | g.74259671G= | CA2146964482 | VSX2 | c.649G= (p.Ala217=)
| |
| 14 | g.74259671G>T | CA390369276 | VSX2 | c.649G>T (p.Ala217Ser)
| |
| 14 | g.74259672C>A | CA390369277 | VSX2 | c.650C>A (p.Ala217Glu)
| |
| 14 | g.74259672C= | CA2146964483 | VSX2 | c.650C= (p.Ala217=)
| |
| 14 | g.74259672C>G | CA390369278 | VSX2 | c.650C>G (p.Ala217Gly)
| |
| 14 | g.74259672C>T | CA10604600 | VSX2 | c.650C>T (p.Ala217Val)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259673G>A | CA7266404 | VSX2 | c.651G>A (p.Ala217=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259673G>C | CA487155869 | VSX2 | c.651G>C (p.Ala217=)
| |
| 14 | g.74259673G= | CA2146964484 | VSX2 | c.651G= (p.Ala217=)
| |
| 14 | g.74259673G>T | CA487155870 | VSX2 | c.651G>T (p.Ala217=)
| COSMIC |
| 14 | g.74259674G>A | CA263556566 | VSX2 | c.652G>A (p.Glu218Lys)
| dbSNP |
| 14 | g.74259674G>C | CA390369279 | VSX2 | c.652G>C (p.Glu218Gln)
| |
| 14 | g.74259674G= | CA2146964485 | VSX2 | c.652G= (p.Glu218=)
| |
| 14 | g.74259674G>T | CA390369280 | VSX2 | c.652G>T (p.Glu218Ter)
| |
| 14 | g.74259675A>C | CA390369281 | VSX2 | c.653A>C (p.Glu218Ala)
| |
| 14 | g.74259675A>G | CA390369282 | VSX2 | c.653A>G (p.Glu218Gly)
| gnomAD v4 |
| 14 | g.74259675A>T | CA390369283 | VSX2 | c.653A>T (p.Glu218Val)
| |
| 14 | g.74259676G>A | CA7266406 | VSX2 | c.654G>A (p.Glu218=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.74259676G>C | CA390369284 | VSX2 | c.654G>C (p.Glu218Asp)
| |
| 14 | g.74259676G= | CA2146964486 | VSX2 | c.654G= (p.Glu218=)
| |
| 14 | g.74259676G>T | CA7266405 | VSX2 | c.654G>T (p.Glu218Asp)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259677T>A | CA390369285 | VSX2 | c.655T>A (p.Tyr219Asn)
| |
| 14 | g.74259677T>C | CA390369286 | VSX2 | c.655T>C (p.Tyr219His)
| |
| 14 | g.74259677T>G | CA390369287 | VSX2 | c.655T>G (p.Tyr219Asp)
| dbSNP |
| 14 | g.74259677T= | CA2146964487 | VSX2 | c.655T= (p.Tyr219=)
| |
| 14 | g.74259678A>C | CA390369288 | VSX2 | c.656A>C (p.Tyr219Ser)
| |
| 14 | g.74259678A>G | CA390369289 | VSX2 | c.656A>G (p.Tyr219Cys)
| |
| 14 | g.74259678A>T | CA390369290 | VSX2 | c.656A>T (p.Tyr219Phe)
| |
| 14 | g.74259678_74259681dup | CA2625651044 | VSX2 | c.656_659dup (p.Leu221TrpfsTer?)
| gnomAD v4 |
| 14 | g.74259679T>A | CA390369291 | VSX2 | c.657T>A (p.Tyr219Ter)
| |
| 14 | g.74259679T>C | CA487155876 | VSX2 | c.657T>C (p.Tyr219=)
| dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.74259679T>G | CA390369292 | VSX2 | c.657T>G (p.Tyr219Ter)
| |
| 14 | g.74259679T= | CA2146964488 | VSX2 | c.657T= (p.Tyr219=)
| |
| 14 | g.74259680G>A | CA390369293 | VSX2 | c.658G>A (p.Gly220Arg)
| |
| 14 | g.74259680G>C | CA390369294 | VSX2 | c.658G>C (p.Gly220Arg)
| |
| 14 | g.74259680G>T | CA390369295 | VSX2 | c.658G>T (p.Gly220Trp)
| |
| 14 | g.74259681G>A | CA390369296 | VSX2 | c.659G>A (p.Gly220Glu)
| |
| 14 | g.74259681G>C | CA390369297 | VSX2 | c.659G>C (p.Gly220Ala)
| |
| 14 | g.74259681G>T | CA390369298 | VSX2 | c.659G>T (p.Gly220Val)
| gnomAD v4 |
| 14 | g.74259682G>A | CA487155880 | VSX2 | c.660G>A (p.Gly220=)
| ClinVar dbSNP gnomAD v4 |
| 14 | g.74259682G>C | CA487155881 | VSX2 | c.660G>C (p.Gly220=)
| |
| 14 | g.74259682G= | CA2146964489 | VSX2 | c.660G= (p.Gly220=)
| |
| 14 | g.74259682G>T | CA487155882 | VSX2 | c.660G>T (p.Gly220=)
| |
| 14 | g.74259683C>A | CA390369300 | VSX2 | c.661C>A (p.Leu221Ile)
| COSMIC |
| 14 | g.74259683C>G | CA390369301 | VSX2 | c.661C>G (p.Leu221Val)
| |
| 14 | g.74259683C>T | CA390369299 | VSX2 | c.661C>T (p.Leu221Phe)
| |
| 14 | g.74259684T>A | CA390369302 | VSX2 | c.662T>A (p.Leu221His)
| |
| 14 | g.74259684T>C | CA390369303 | VSX2 | c.662T>C (p.Leu221Pro)
| |
| 14 | g.74259684T>G | CA390369304 | VSX2 | c.662T>G (p.Leu221Arg)
| |
| 14 | g.74259685C>A | CA487155885 | VSX2 | c.663C>A (p.Leu221=)
| |
| 14 | g.74259685C>G | CA487155886 | VSX2 | c.663C>G (p.Leu221=)
| gnomAD v4 |
| 14 | g.74259685C>T | CA487155887 | VSX2 | c.663C>T (p.Leu221=)
| |
| 14 | g.74259686T>A | CA390369305 | VSX2 | c.664T>A (p.Tyr222Asn)
| |
| 14 | g.74259686T>C | CA390369306 | VSX2 | c.664T>C (p.Tyr222His)
| dbSNP |
| 14 | g.74259686T>G | CA390369307 | VSX2 | c.664T>G (p.Tyr222Asp)
| |
| 14 | g.74259686T= | CA2146964490 | VSX2 | c.664T= (p.Tyr222=)
| |
| 14 | g.74259686dup | CA2580088747 | VSX2 | c.664dup (p.Tyr222LeufsTer?)
| ClinVar |
| 14 | g.74259687A>C | CA390369308 | VSX2 | c.665A>C (p.Tyr222Ser)
| |
| 14 | g.74259687A>G | CA390369309 | VSX2 | c.665A>G (p.Tyr222Cys)
| |
| 14 | g.74259687A>T | CA390369310 | VSX2 | c.665A>T (p.Tyr222Phe)
| |
| 14 | g.74259688C>A | CA390369311 | VSX2 | c.666C>A (p.Tyr222Ter)
| |
| 14 | g.74259688C= | CA2146964491 | VSX2 | c.666C= (p.Tyr222=)
| |
| 14 | g.74259688C>G | CA390369312 | VSX2 | c.666C>G (p.Tyr222Ter)
| |
| 14 | g.74259688C>T | CA7266407 | VSX2 | c.666C>T (p.Tyr222=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259689G>A | CA071309 | VSX2 | c.667G>A (p.Gly223Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.74259689G>C | CA390369313 | VSX2 | c.667G>C (p.Gly223Arg)
| ClinVar |
| 14 | g.74259689G= | CA2146964492 | VSX2 | c.667G= (p.Gly223=)
| |
| 14 | g.74259689G>T | CA390369314 | VSX2 | c.667G>T (p.Gly223Trp)
| |
| 14 | g.74259692del | CA645584357 | VSX2 | c.670del (p.Ala224ProfsTer?)
| COSMIC |
| 14 | g.74259690G>A | CA390369315 | VSX2 | c.668G>A (p.Gly223Glu)
| |
| 14 | g.74259690G>C | CA390369316 | VSX2 | c.668G>C (p.Gly223Ala)
| |
| 14 | g.74259690G>T | CA390369317 | VSX2 | c.668G>T (p.Gly223Val)
| |
| 14 | g.74259691G>A | CA487155894 | VSX2 | c.669G>A (p.Gly223=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259691G>C | CA487155892 | VSX2 | c.669G>C (p.Gly223=)
| |
| 14 | g.74259691G= | CA2146964493 | VSX2 | c.669G= (p.Gly223=)
| |
| 14 | g.74259691G>T | CA487155893 | VSX2 | c.669G>T (p.Gly223=)
| ClinVar |
| 14 | g.74259692G>A | CA390369318 | VSX2 | c.670G>A (p.Ala224Thr)
| |
| 14 | g.74259692G>C | CA390369319 | VSX2 | c.670G>C (p.Ala224Pro)
| |
| 14 | g.74259692G>T | CA390369320 | VSX2 | c.670G>T (p.Ala224Ser)
| |
| 14 | g.74259693C>A | CA390369321 | VSX2 | c.671C>A (p.Ala224Asp)
| dbSNP gnomAD v4 |
| 14 | g.74259693C= | CA2146964494 | VSX2 | c.671C= (p.Ala224=)
| |
| 14 | g.74259693C>G | CA390369322 | VSX2 | c.671C>G (p.Ala224Gly)
| |
| 14 | g.74259693C>T | CA390369323 | VSX2 | c.671C>T (p.Ala224Val)
| COSMIC |
| 14 | g.74259694C>A | CA487155898 | VSX2 | c.672C>A (p.Ala224=)
| |
| 14 | g.74259694C>G | CA487155899 | VSX2 | c.672C>G (p.Ala224=)
| |
| 14 | g.74259694C>T | CA487155900 | VSX2 | c.672C>T (p.Ala224=)
| gnomAD v4 COSMIC |
| 14 | g.74259695A= | CA2146964495 | VSX2 | c.673A= (p.Met225=)
| |
| 14 | g.74259695A>C | CA390369324 | VSX2 | c.673A>C (p.Met225Leu)
| |
| 14 | g.74259695A>G | CA7266408 | VSX2 | c.673A>G (p.Met225Val)
| dbSNP ExAC gnomAD v3 gnomAD v4 |
| 14 | g.74259695A>T | CA390369325 | VSX2 | c.673A>T (p.Met225Leu)
| dbSNP |
| 14 | g.74259696T>A | CA390369327 | VSX2 | c.674T>A (p.Met225Lys)
| |
| 14 | g.74259696T>C | CA390369328 | VSX2 | c.674T>C (p.Met225Thr)
| gnomAD v4 |
| 14 | g.74259696T>G | CA390369326 | VSX2 | c.674T>G (p.Met225Arg)
| |
| 14 | g.74259697G>A | CA390369330 | VSX2 | c.675G>A (p.Met225Ile)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259697G>C | CA390369329 | VSX2 | c.675G>C (p.Met225Ile)
| |
| 14 | g.74259697G= | CA2146964496 | VSX2 | c.675G= (p.Met225=)
| |
| 14 | g.74259697G>T | CA390369331 | VSX2 | c.675G>T (p.Met225Ile)
| |
| 14 | g.74259698G>A | CA390369332 | VSX2 | c.676G>A (p.Val226Met)
| gnomAD v4 |
| 14 | g.74259698G>C | CA390369334 | VSX2 | c.676G>C (p.Val226Leu)
| |
| 14 | g.74259698G>T | CA390369333 | VSX2 | c.676G>T (p.Val226Leu)
| |
| 14 | g.74259699T>A | CA390369335 | VSX2 | c.677T>A (p.Val226Glu)
| |
| 14 | g.74259699T>C | CA390369336 | VSX2 | c.677T>C (p.Val226Ala)
| |
| 14 | g.74259699T>G | CA390369337 | VSX2 | c.677T>G (p.Val226Gly)
| |
| 14 | g.74259700G>A | CA487155905 | VSX2 | c.678G>A (p.Val226=)
| gnomAD v4 |
| 14 | g.74259700G>C | CA487155906 | VSX2 | c.678G>C (p.Val226=)
| |
| 14 | g.74259700G>T | CA487155907 | VSX2 | c.678G>T (p.Val226=)
| |
| 14 | g.74259701C>A | CA487155908 | VSX2 | c.679C>A (p.Arg227=)
| |
| 14 | g.74259701C= | CA2146964497 | VSX2 | c.679C= (p.Arg227=)
| |
| 14 | g.74259701C>G | CA390369338 | VSX2 | c.679C>G (p.Arg227Gly)
| |
| 14 | g.74259701C>T | CA124414 | VSX2 | c.679C>T (p.Arg227Trp)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259702G>A | CA390369339 | VSX2 | c.680G>A (p.Arg227Gln)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259702G>C | CA390369340 | VSX2 | c.680G>C (p.Arg227Pro)
| |
| 14 | g.74259702G= | CA2146964498 | VSX2 | c.680G= (p.Arg227=)
| |
| 14 | g.74259702G>T | CA390369341 | VSX2 | c.680G>T (p.Arg227Leu)
| |
| 14 | g.74259703G>A | CA487155910 | VSX2 | c.681G>A (p.Arg227=)
| |
| 14 | g.74259703G>C | CA487155912 | VSX2 | c.681G>C (p.Arg227=)
| |
| 14 | g.74259703G>T | CA487155911 | VSX2 | c.681G>T (p.Arg227=)
| |
| 14 | g.74259704C>A | CA390369342 | VSX2 | c.682C>A (p.His228Asn)
| |
| 14 | g.74259704C>G | CA390369344 | VSX2 | c.682C>G (p.His228Asp)
| |
| 14 | g.74259704C>T | CA390369343 | VSX2 | c.682C>T (p.His228Tyr)
| |
| 14 | g.74259705A>C | CA390369345 | VSX2 | c.683A>C (p.His228Pro)
| |
| 14 | g.74259705A>G | CA390369346 | VSX2 | c.683A>G (p.His228Arg)
| |
| 14 | g.74259705A>T | CA390369347 | VSX2 | c.683A>T (p.His228Leu)
| |
| 14 | g.74259706C>A | CA390369348 | VSX2 | c.684C>A (p.His228Gln)
| |
| 14 | g.74259706C= | CA2146964499 | VSX2 | c.684C= (p.His228=)
| |
| 14 | g.74259706C>G | CA390369349 | VSX2 | c.684C>G (p.His228Gln)
| |
| 14 | g.74259706C>T | CA487155914 | VSX2 | c.684C>T (p.His228=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259707T>A | CA7266409 | VSX2 | c.685T>A (p.Ser229Thr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.74259707T>C | CA390369351 | VSX2 | c.685T>C (p.Ser229Pro)
| |
| 14 | g.74259707T>G | CA390369350 | VSX2 | c.685T>G (p.Ser229Ala)
| |
| 14 | g.74259707T= | CA2146964500 | VSX2 | c.685T= (p.Ser229=)
| |
| 14 | g.74259708C>A | CA390369352 | VSX2 | c.686C>A (p.Ser229Tyr)
| |
| 14 | g.74259708C>G | CA390369353 | VSX2 | c.686C>G (p.Ser229Cys)
| |
| 14 | g.74259708C>T | CA390369354 | VSX2 | c.686C>T (p.Ser229Phe)
| |
| 14 | g.74259709C>A | CA487155918 | VSX2 | c.687C>A (p.Ser229=)
| |
| 14 | g.74259709C= | CA2146964501 | VSX2 | c.687C= (p.Ser229=)
| |
| 14 | g.74259709C>G | CA487155919 | VSX2 | c.687C>G (p.Ser229=)
| |
| 14 | g.74259709C>T | CA263556600 | VSX2 | c.687C>T (p.Ser229=)
| dbSNP gnomAD v4 |
| 14 | g.74259710A>C | CA390369355 | VSX2 | c.688A>C (p.Ile230Leu)
| |
| 14 | g.74259710A>G | CA390369356 | VSX2 | c.688A>G (p.Ile230Val)
| |
| 14 | g.74259710A>T | CA390369357 | VSX2 | c.688A>T (p.Ile230Phe)
| |
| 14 | g.74259711del | CA2695219548 | VSX2 | c.689del (p.Ile230ThrfsTer?)
| |
| 14 | g.74259711T>A | CA390369358 | VSX2 | c.689T>A (p.Ile230Asn)
| |
| 14 | g.74259711T>C | CA390369359 | VSX2 | c.689T>C (p.Ile230Thr)
| gnomAD v4 COSMIC |
| 14 | g.74259711T>G | CA390369360 | VSX2 | c.689T>G (p.Ile230Ser)
| gnomAD v4 |
| 14 | g.74259711T= | CA2146964502 | VSX2 | c.689T= (p.Ile230=)
| |
| 14 | g.74259712C>A | CA487155920 | VSX2 | c.690C>A (p.Ile230=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259712C= | CA2146964503 | VSX2 | c.690C= (p.Ile230=)
| |
| 14 | g.74259712C>G | CA390369361 | VSX2 | c.690C>G (p.Ile230Met)
| |
| 14 | g.74259712C>T | CA7266411 | VSX2 | c.690C>T (p.Ile230=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.74259716dup | CA7266410 | VSX2 | c.694dup (p.Leu232ProfsTer?)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.74259713C>A | CA390369362 | VSX2 | c.691C>A (p.Pro231Thr)
| |
| 14 | g.74259713C= | CA2146964504 | VSX2 | c.691C= (p.Pro231=)
| |
| 14 | g.74259713C>G | CA390369363 | VSX2 | c.691C>G (p.Pro231Ala)
| |
| 14 | g.74259713C>T | CA263556621 | VSX2 | c.691C>T (p.Pro231Ser)
| dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.74259714C>A | CA390369364 | VSX2 | c.692C>A (p.Pro231His)
| |
| 14 | g.74259714C>G | CA390369365 | VSX2 | c.692C>G (p.Pro231Arg)
| |
| 14 | g.74259714C>T | CA390369366 | VSX2 | c.692C>T (p.Pro231Leu)
| |
| 14 | g.74259715C>A | CA487155924 | VSX2 | c.693C>A (p.Pro231=)
| |
| 14 | g.74259715C= | CA2146964505 | VSX2 | c.693C= (p.Pro231=)
| |
| 14 | g.74259715C>G | CA7266412 | VSX2 | c.693C>G (p.Pro231=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.74259715C>T | CA487155926 | VSX2 | c.693C>T (p.Pro231=)
| gnomAD v4 COSMIC |
| 14 | g.74259716C>A | CA390369367 | VSX2 | c.694C>A (p.Leu232Met)
| |
| 14 | g.74259716C= | CA2146964506 | VSX2 | c.694C= (p.Leu232=)
| |
| 14 | g.74259716C>G | CA390369368 | VSX2 | c.694C>G (p.Leu232Val)
| |
| 14 | g.74259716C>T | CA487155928 | VSX2 | c.694C>T (p.Leu232=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259717T>A | CA390369369 | VSX2 | c.695T>A (p.Leu232Gln)
| |
| 14 | g.74259717T>C | CA390369370 | VSX2 | c.695T>C (p.Leu232Pro)
| |
| 14 | g.74259717T>G | CA390369371 | VSX2 | c.695T>G (p.Leu232Arg)
| |
| 14 | g.74259718G>A | CA487155930 | VSX2 | c.696G>A (p.Leu232=)
| ClinVar |
| 14 | g.74259718G>C | CA487155931 | VSX2 | c.696G>C (p.Leu232=)
| |
| 14 | g.74259718G>T | CA487155932 | VSX2 | c.696G>T (p.Leu232=)
| |
| 14 | g.74259719C>A | CA390369372 | VSX2 | c.697C>A (p.Pro233Thr)
| |
| 14 | g.74259719C>G | CA390369373 | VSX2 | c.697C>G (p.Pro233Ala)
| |
| 14 | g.74259719C>T | CA390369374 | VSX2 | c.697C>T (p.Pro233Ser)
| |
| 14 | g.74259720C>A | CA390369377 | VSX2 | c.698C>A (p.Pro233His)
| |
| 14 | g.74259720C>G | CA390369376 | VSX2 | c.698C>G (p.Pro233Arg)
| |
| 14 | g.74259720C>T | CA390369375 | VSX2 | c.698C>T (p.Pro233Leu)
| |
| 14 | g.74259721C>A | CA487155936 | VSX2 | c.699C>A (p.Pro233=)
| gnomAD v4 |
| 14 | g.74259721C= | CA2146964507 | VSX2 | c.699C= (p.Pro233=)
| |
| 14 | g.74259721C>G | CA487155937 | VSX2 | c.699C>G (p.Pro233=)
| |
| 14 | g.74259721C>T | CA7266413 | VSX2 | c.699C>T (p.Pro233=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259722G>A | CA7266414 | VSX2 | c.700G>A (p.Glu234Lys)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259722G>C | CA390369378 | VSX2 | c.700G>C (p.Glu234Gln)
| |
| 14 | g.74259722G= | CA2146964508 | VSX2 | c.700G= (p.Glu234=)
| |
| 14 | g.74259722G>T | CA390369379 | VSX2 | c.700G>T (p.Glu234Ter)
| gnomAD v4 |
| 14 | g.74259723A= | CA2146964509 | VSX2 | c.701A= (p.Glu234=)
| |
| 14 | g.74259723A>C | CA390369380 | VSX2 | c.701A>C (p.Glu234Ala)
| |
| 14 | g.74259723A>G | CA390369381 | VSX2 | c.701A>G (p.Glu234Gly)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.74259723A>T | CA390369382 | VSX2 | c.701A>T (p.Glu234Val)
| |
| 14 | g.74259724G>A | CA487155938 | VSX2 | c.702G>A (p.Glu234=)
| ClinVar gnomAD v4 |
| 14 | g.74259724G>C | CA390369383 | VSX2 | c.702G>C (p.Glu234Asp)
| |
| 14 | g.74259724G>T | CA390369384 | VSX2 | c.702G>T (p.Glu234Asp)
| |
| 14 | g.74259725T>A | CA390369385 | VSX2 | c.703T>A (p.Ser235Thr)
| |
| 14 | g.74259725T>C | CA390369386 | VSX2 | c.703T>C (p.Ser235Pro)
| |
| 14 | g.74259725T>G | CA390369387 | VSX2 | c.703T>G (p.Ser235Ala)
| |
| 14 | g.74259726C>A | CA390369388 | VSX2 | c.704C>A (p.Ser235Tyr)
| |
| 14 | g.74259726C>G | CA390369390 | VSX2 | c.704C>G (p.Ser235Cys)
| |
| 14 | g.74259726C>T | CA390369389 | VSX2 | c.704C>T (p.Ser235Phe)
| |
| 14 | g.74259727C>A | CA487155940 | VSX2 | c.705C>A (p.Ser235=)
| |
| 14 | g.74259727C>G | CA487155941 | VSX2 | c.705C>G (p.Ser235=)
| |
| 14 | g.74259727C>T | CA487155942 | VSX2 | c.705C>T (p.Ser235=)
| COSMIC |
| 14 | g.74259728A>C | CA390369391 | VSX2 | c.706A>C (p.Ile236Leu)
| |
| 14 | g.74259728A>G | CA390369393 | VSX2 | c.706A>G (p.Ile236Val)
| gnomAD v4 |
| 14 | g.74259728A>T | CA390369392 | VSX2 | c.706A>T (p.Ile236Phe)
| |
| 14 | g.74259728_74259731delinsATCC | CA2146964510 | VSX2 | c.706_709delinsATCC (p.Ile236=)
| |
| 14 | g.74259729T>A | CA390369394 | VSX2 | c.707T>A (p.Ile236Asn)
| |
| 14 | g.74259729T>C | CA390369395 | VSX2 | c.707T>C (p.Ile236Thr)
| |
| 14 | g.74259729T>G | CA390369396 | VSX2 | c.707T>G (p.Ile236Ser)
| |
| 14 | g.74259731_74259733del | CA2146964511 | VSX2 | c.709_711del (p.Leu237del)
| dbSNP |
| 14 | g.74259730C>A | CA487155944 | VSX2 | c.708C>A (p.Ile236=)
| |
| 14 | g.74259730C>G | CA390369397 | VSX2 | c.708C>G (p.Ile236Met)
| |
| 14 | g.74259730C>T | CA487155945 | VSX2 | c.708C>T (p.Ile236=)
| gnomAD v4 |
| 14 | g.74259731C>A | CA390369398 | VSX2 | c.709C>A (p.Leu237Ile)
| |
| 14 | g.74259731C= | CA2146964512 | VSX2 | c.709C= (p.Leu237=)
| |
| 14 | g.74259731C>G | CA390369399 | VSX2 | c.709C>G (p.Leu237Val)
| dbSNP gnomAD v2 |
| 14 | g.74259731C>T | CA390369400 | VSX2 | c.709C>T (p.Leu237Phe)
| |
| 14 | g.74259732T>A | CA390369401 | VSX2 | c.710T>A (p.Leu237His)
| |
| 14 | g.74259732T>C | CA390369402 | VSX2 | c.710T>C (p.Leu237Pro)
| |
| 14 | g.74259732T>G | CA390369403 | VSX2 | c.710T>G (p.Leu237Arg)
| |
| 14 | g.74259733C>A | CA487155950 | VSX2 | c.711C>A (p.Leu237=)
| |
| 14 | g.74259733C>G | CA487155948 | VSX2 | c.711C>G (p.Leu237=)
| gnomAD v4 |
| 14 | g.74259733C>T | CA487155949 | VSX2 | c.711C>T (p.Leu237=)
| ClinVar dbSNP |
| 14 | g.74259734A= | CA2146964513 | VSX2 | c.712A= (p.Lys238=)
| |
| 14 | g.74259734A>C | CA7266415 | VSX2 | c.712A>C (p.Lys238Gln)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259734A>G | CA390369404 | VSX2 | c.712A>G (p.Lys238Glu)
| |
| 14 | g.74259734A>T | CA390369405 | VSX2 | c.712A>T (p.Lys238Ter)
| |
| 14 | g.74259735A>C | CA390369406 | VSX2 | c.713A>C (p.Lys238Thr)
| |
| 14 | g.74259735A>G | CA390369408 | VSX2 | c.713A>G (p.Lys238Arg)
| |
| 14 | g.74259735A>T | CA390369407 | VSX2 | c.713A>T (p.Lys238Met)
| |
| 14 | g.74259736G>A | CA7266416 | VSX2 | c.714G>A (p.Lys238=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.74259736G>C | CA390369409 | VSX2 | c.714G>C (p.Lys238Asn)
| |
| 14 | g.74259736G= | CA2146964514 | VSX2 | c.714G= (p.Lys238=)
| |
| 14 | g.74259736G>T | CA390369410 | VSX2 | c.714G>T (p.Lys238Asn)
| |
| 14 | g.74259737T>A | CA390369411 | VSX2 | c.715T>A (p.Ser239Thr)
| |
| 14 | g.74259737T>C | CA390369412 | VSX2 | c.715T>C (p.Ser239Pro)
| |
| 14 | g.74259737T>G | CA390369413 | VSX2 | c.715T>G (p.Ser239Ala)
| |
| 14 | g.74259738C>A | CA390369414 | VSX2 | c.716C>A (p.Ser239Ter)
| |
| 14 | g.74259738C>G | CA390369415 | VSX2 | c.716C>G (p.Ser239Ter)
| |
| 14 | g.74259738C>T | CA390369416 | VSX2 | c.716C>T (p.Ser239Leu)
| |
| 14 | g.74259739A>C | CA487155953 | VSX2 | c.717A>C (p.Ser239=)
| |
| 14 | g.74259739A>G | CA487155955 | VSX2 | c.717A>G (p.Ser239=)
| dbSNP |
| 14 | g.74259739A>T | CA487155957 | VSX2 | c.717A>T (p.Ser239=)
| gnomAD v4 |
| 14 | g.74259740G>A | CA390369419 | VSX2 | c.718G>A (p.Ala240Thr)
| dbSNP gnomAD v4 COSMIC |
| 14 | g.74259740G>C | CA390369418 | VSX2 | c.718G>C (p.Ala240Pro)
| |
| 14 | g.74259740G= | CA2146964515 | VSX2 | c.718G= (p.Ala240=)
| |
| 14 | g.74259740G>T | CA390369417 | VSX2 | c.718G>T (p.Ala240Ser)
| |
