| 3 | g.129532636C>A | CA354470394 | RHO | c.800C>A (p.Pro267His)
| |
| 3 | g.129532636C= | CA1401211805 | RHO | c.800C= (p.Pro267=)
| |
| 3 | g.129532636C>G | CA354470395 | RHO | c.800C>G (p.Pro267Arg)
| |
| 3 | g.129532636C>T | CA256680 | RHO | c.800C>T (p.Pro267Leu)
| ClinVar dbSNP gnomAD v4 |
| 3 | g.129532637C>A | CA435769107 | RHO | c.801C>A (p.Pro267=)
| |
| 3 | g.129532637C= | CA1401211810 | RHO | c.801C= (p.Pro267=)
| |
| 3 | g.129532637C>G | CA435769108 | RHO | c.801C>G (p.Pro267=)
| |
| 3 | g.129532637C>T | CA435769109 | RHO | c.801C>T (p.Pro267=)
| dbSNP gnomAD v4 |
| 3 | g.129532638T>A | CA354470396 | RHO | c.802T>A (p.Tyr268Asn)
| |
| 3 | g.129532638T>C | CA354470398 | RHO | c.802T>C (p.Tyr268His)
| |
| 3 | g.129532638T>G | CA354470397 | RHO | c.802T>G (p.Tyr268Asp)
| |
| 3 | g.129532639A>C | CA354470399 | RHO | c.803A>C (p.Tyr268Ser)
| |
| 3 | g.129532639A>G | CA354470400 | RHO | c.803A>G (p.Tyr268Cys)
| |
| 3 | g.129532639A>T | CA354470402 | RHO | c.803A>T (p.Tyr268Phe)
| |
| 3 | g.129532640C>A | CA354470404 | RHO | c.804C>A (p.Tyr268Ter)
| |
| 3 | g.129532640C= | CA1401211817 | RHO | c.804C= (p.Tyr268=)
| |
| 3 | g.129532640C>G | CA354470406 | RHO | c.804C>G (p.Tyr268Ter)
| |
| 3 | g.129532640C>T | CA2607289 | RHO | c.804C>T (p.Tyr268=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532641_129532643dup | CA2577961805 | RHO | c.805_807dup (p.Ala269_Ser270insAla)
| |
| 3 | g.129532641G>A | CA2607290 | RHO | c.805G>A (p.Ala269Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532641G>C | CA354470409 | RHO | c.805G>C (p.Ala269Pro)
| |
| 3 | g.129532641G= | CA1401211824 | RHO | c.805G= (p.Ala269=)
| |
| 3 | g.129532641G>T | CA354470410 | RHO | c.805G>T (p.Ala269Ser)
| |
| 3 | g.129532642C>A | CA354470412 | RHO | c.806C>A (p.Ala269Asp)
| ClinVar dbSNP |
| 3 | g.129532642C= | CA1401211831 | RHO | c.806C= (p.Ala269=)
| |
| 3 | g.129532642C>G | CA354470413 | RHO | c.806C>G (p.Ala269Gly)
| |
| 3 | g.129532642C>T | CA354470414 | RHO | c.806C>T (p.Ala269Val)
| |
| 3 | g.129532643C>A | CA435769118 | RHO | c.807C>A (p.Ala269=)
| |
| 3 | g.129532643C>G | CA435769119 | RHO | c.807C>G (p.Ala269=)
| |
| 3 | g.129532643C>T | CA435769120 | RHO | c.807C>T (p.Ala269=)
| gnomAD v4 |
| 3 | g.129532644A= | CA1401211839 | RHO | c.808A= (p.Ser270=)
| |
| 3 | g.129532644A>C | CA16609650 | RHO | c.808A>C (p.Ser270Arg)
| ClinVar dbSNP |
| 3 | g.129532644A>G | CA354470418 | RHO | c.808A>G (p.Ser270Gly)
| |
| 3 | g.129532644A>T | CA354470417 | RHO | c.808A>T (p.Ser270Cys)
| |
| 3 | g.129532645G>A | CA354470420 | RHO | c.809G>A (p.Ser270Asn)
| COSMIC |
| 3 | g.129532645G>C | CA354470422 | RHO | c.809G>C (p.Ser270Thr)
| |
| 3 | g.129532645G>T | CA354470423 | RHO | c.809G>T (p.Ser270Ile)
| |
| 3 | g.129532646C>A | CA354470425 | RHO | c.810C>A (p.Ser270Arg)
| ClinVar dbSNP |
| 3 | g.129532646C= | CA1401211845 | RHO | c.810C= (p.Ser270=)
| |
| 3 | g.129532646C>G | CA354470426 | RHO | c.810C>G (p.Ser270Arg)
| |
| 3 | g.129532646C>T | CA2607291 | RHO | c.810C>T (p.Ser270=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.129532647G>A | CA2607292 | RHO | c.811G>A (p.Val271Met)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.129532647G>C | CA354470430 | RHO | c.811G>C (p.Val271Leu)
| |
| 3 | g.129532647G= | CA1401211852 | RHO | c.811G= (p.Val271=)
| |
| 3 | g.129532647G>T | CA354470431 | RHO | c.811G>T (p.Val271Leu)
| |
| 3 | g.129532648T>A | CA354470433 | RHO | c.812T>A (p.Val271Glu)
| |
| 3 | g.129532648T>C | CA354470435 | RHO | c.812T>C (p.Val271Ala)
| |
| 3 | g.129532648T>G | CA354470436 | RHO | c.812T>G (p.Val271Gly)
| |
| 3 | g.129532649G>A | CA435769125 | RHO | c.813G>A (p.Val271=)
| |
| 3 | g.129532649G>C | CA435769126 | RHO | c.813G>C (p.Val271=)
| dbSNP |
| 3 | g.129532649G= | CA1401211855 | RHO | c.813G= (p.Val271=)
| |
| 3 | g.129532649G>T | CA435769127 | RHO | c.813G>T (p.Val271=)
| |
| 3 | g.129532650G>A | CA354470441 | RHO | c.814G>A (p.Ala272Thr)
| dbSNP gnomAD v4 |
| 3 | g.129532650G>C | CA354470439 | RHO | c.814G>C (p.Ala272Pro)
| |
| 3 | g.129532650G= | CA1401211860 | RHO | c.814G= (p.Ala272=)
| |
| 3 | g.129532650G>T | CA354470438 | RHO | c.814G>T (p.Ala272Ser)
| |
| 3 | g.129532651del | CA2567976588 | RHO | c.815del (p.Ala272AspfsTer17)
| |
| 3 | g.129532651C>A | CA354470443 | RHO | c.815C>A (p.Ala272Glu)
| |
| 3 | g.129532651C>G | CA354470445 | RHO | c.815C>G (p.Ala272Gly)
| |
| 3 | g.129532651C>T | CA354470444 | RHO | c.815C>T (p.Ala272Val)
| gnomAD v4 |
| 3 | g.129532652A>C | CA435769131 | RHO | c.816A>C (p.Ala272=)
| dbSNP |
| 3 | g.129532652A>G | CA435769133 | RHO | c.816A>G (p.Ala272=)
| |
| 3 | g.129532652A>T | CA435769134 | RHO | c.816A>T (p.Ala272=)
| ClinVar gnomAD v4 |
| 3 | g.129532653T>A | CA354470447 | RHO | c.817T>A (p.Phe273Ile)
| |
| 3 | g.129532653T>C | CA354470457 | RHO | c.817T>C (p.Phe273Leu)
| |
| 3 | g.129532653T>G | CA354470459 | RHO | c.817T>G (p.Phe273Val)
| |
| 3 | g.129532654T>A | CA354470461 | RHO | c.818T>A (p.Phe273Tyr)
| |
| 3 | g.129532654T>C | CA354470462 | RHO | c.818T>C (p.Phe273Ser)
| |
| 3 | g.129532654T>G | CA354470463 | RHO | c.818T>G (p.Phe273Cys)
| |
| 3 | g.129532655C>A | CA354470465 | RHO | c.819C>A (p.Phe273Leu)
| |
| 3 | g.129532655C>G | CA354470467 | RHO | c.819C>G (p.Phe273Leu)
| |
| 3 | g.129532655C>T | CA435769137 | RHO | c.819C>T (p.Phe273=)
| |
| 3 | g.129532656T>A | CA354470468 | RHO | c.820T>A (p.Tyr274Asn)
| |
| 3 | g.129532656T>C | CA354470470 | RHO | c.820T>C (p.Tyr274His)
| |
| 3 | g.129532656T>G | CA354470472 | RHO | c.820T>G (p.Tyr274Asp)
| |
| 3 | g.129532657A>C | CA354470477 | RHO | c.821A>C (p.Tyr274Ser)
| |
| 3 | g.129532657A>G | CA354470475 | RHO | c.821A>G (p.Tyr274Cys)
| |
| 3 | g.129532657A>T | CA354470474 | RHO | c.821A>T (p.Tyr274Phe)
| gnomAD v4 |
| 3 | g.129532658C>A | CA354470479 | RHO | c.822C>A (p.Tyr274Ter)
| |
| 3 | g.129532658C= | CA1401211862 | RHO | c.822C= (p.Tyr274=)
| |
| 3 | g.129532658C>G | CA354470480 | RHO | c.822C>G (p.Tyr274Ter)
| |
| 3 | g.129532658C>T | CA435769142 | RHO | c.822C>T (p.Tyr274=)
| dbSNP gnomAD v4 |
| 3 | g.129532659A= | CA1401211864 | RHO | c.823A= (p.Ile275=)
| |
| 3 | g.129532659A>C | CA354470482 | RHO | c.823A>C (p.Ile275Leu)
| ClinVar dbSNP |
| 3 | g.129532659A>G | CA2607293 | RHO | c.823A>G (p.Ile275Val)
| dbSNP ExAC gnomAD v2 |
| 3 | g.129532659A>T | CA354470484 | RHO | c.823A>T (p.Ile275Phe)
| |
| 3 | g.129532660T>A | CA354470486 | RHO | c.824T>A (p.Ile275Asn)
| |
| 3 | g.129532660T>C | CA354470487 | RHO | c.824T>C (p.Ile275Thr)
| |
| 3 | g.129532660T>G | CA354470488 | RHO | c.824T>G (p.Ile275Ser)
| |
| 3 | g.129532661C>A | CA435769145 | RHO | c.825C>A (p.Ile275=)
| dbSNP |
| 3 | g.129532661C= | CA1401211869 | RHO | c.825C= (p.Ile275=)
| |
| 3 | g.129532661C>G | CA354470489 | RHO | c.825C>G (p.Ile275Met)
| |
| 3 | g.129532661C>T | CA435769146 | RHO | c.825C>T (p.Ile275=)
| gnomAD v4 |
| 3 | g.129532662T>A | CA354470490 | RHO | c.826T>A (p.Phe276Ile)
| |
| 3 | g.129532662T>C | CA354470492 | RHO | c.826T>C (p.Phe276Leu)
| |
| 3 | g.129532662T>G | CA2607294 | RHO | c.826T>G (p.Phe276Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532662T= | CA1401211877 | RHO | c.826T= (p.Phe276=)
| |
| 3 | g.129532663T>A | CA354470497 | RHO | c.827T>A (p.Phe276Tyr)
| |
| 3 | g.129532663T>C | CA354470496 | RHO | c.827T>C (p.Phe276Ser)
| |
| 3 | g.129532663T>G | CA354470494 | RHO | c.827T>G (p.Phe276Cys)
| |
| 3 | g.129532664C>A | CA354470499 | RHO | c.828C>A (p.Phe276Leu)
| |
| 3 | g.129532664C= | CA1401211884 | RHO | c.828C= (p.Phe276=)
| |
| 3 | g.129532664C>G | CA354470501 | RHO | c.828C>G (p.Phe276Leu)
| |
| 3 | g.129532664C>T | CA2607295 | RHO | c.828C>T (p.Phe276=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.129532665A>C | CA354470503 | RHO | c.829A>C (p.Thr277Pro)
| |
| 3 | g.129532665A>G | CA354470504 | RHO | c.829A>G (p.Thr277Ala)
| |
| 3 | g.129532665A>T | CA354470505 | RHO | c.829A>T (p.Thr277Ser)
| |
| 3 | g.129532666C>A | CA354470507 | RHO | c.830C>A (p.Thr277Asn)
| |
| 3 | g.129532666C>G | CA354470508 | RHO | c.830C>G (p.Thr277Ser)
| |
| 3 | g.129532666C>T | CA354470509 | RHO | c.830C>T (p.Thr277Ile)
| gnomAD v4 |
| 3 | g.129532667C>A | CA82620788 | RHO | c.831C>A (p.Thr277=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.129532667C= | CA1401211888 | RHO | c.831C= (p.Thr277=)
| |
| 3 | g.129532667C>G | CA435769150 | RHO | c.831C>G (p.Thr277=)
| |
| 3 | g.129532667C>T | CA435769152 | RHO | c.831C>T (p.Thr277=)
| |
| 3 | g.129532668C>A | CA354470511 | RHO | c.832C>A (p.His278Asn)
| |
| 3 | g.129532668C>G | CA354470512 | RHO | c.832C>G (p.His278Asp)
| |
| 3 | g.129532668C>T | CA354470514 | RHO | c.832C>T (p.His278Tyr)
| |
| 3 | g.129532669A>C | CA354470517 | RHO | c.833A>C (p.His278Pro)
| ClinVar dbSNP |
| 3 | g.129532669A>G | CA354470518 | RHO | c.833A>G (p.His278Arg)
| |
| 3 | g.129532669A>T | CA354470516 | RHO | c.833A>T (p.His278Leu)
| |
| 3 | g.129532670C>A | CA354470519 | RHO | c.834C>A (p.His278Gln)
| |
| 3 | g.129532670C>G | CA354470520 | RHO | c.834C>G (p.His278Gln)
| |
| 3 | g.129532670C>T | CA435769158 | RHO | c.834C>T (p.His278=)
| |
| 3 | g.129532671C>A | CA354470521 | RHO | c.835C>A (p.Gln279Lys)
| |
| 3 | g.129532671C>G | CA354470522 | RHO | c.835C>G (p.Gln279Glu)
| gnomAD v4 |
| 3 | g.129532671C>T | CA354470524 | RHO | c.835C>T (p.Gln279Ter)
| |
| 3 | g.129532672A= | CA1401211892 | RHO | c.836A= (p.Gln279=)
| |
| 3 | g.129532672A>C | CA354470529 | RHO | c.836A>C (p.Gln279Pro)
| ClinVar dbSNP gnomAD v4 |
| 3 | g.129532672A>G | CA354470526 | RHO | c.836A>G (p.Gln279Arg)
| |
| 3 | g.129532672A>T | CA354470527 | RHO | c.836A>T (p.Gln279Leu)
| |
| 3 | g.129532673G>A | CA435769161 | RHO | c.837G>A (p.Gln279=)
| |
| 3 | g.129532673G>C | CA354470530 | RHO | c.837G>C (p.Gln279His)
| |
| 3 | g.129532673G>T | CA354470532 | RHO | c.837G>T (p.Gln279His)
| |
| 3 | g.129532674G>A | CA354470534 | RHO | c.838G>A (p.Gly280Ser)
| |
| 3 | g.129532674G>C | CA354470535 | RHO | c.838G>C (p.Gly280Arg)
| |
| 3 | g.129532674G>T | CA354470537 | RHO | c.838G>T (p.Gly280Cys)
| |
| 3 | g.129532675G>A | CA354470542 | RHO | c.839G>A (p.Gly280Asp)
| |
| 3 | g.129532675G>C | CA354470541 | RHO | c.839G>C (p.Gly280Ala)
| |
| 3 | g.129532675G>T | CA354470539 | RHO | c.839G>T (p.Gly280Val)
| |
| 3 | g.129532676C>A | CA435769165 | RHO | c.840C>A (p.Gly280=)
| COSMIC |
| 3 | g.129532676C>G | CA435769166 | RHO | c.840C>G (p.Gly280=)
| |
| 3 | g.129532676C>T | CA435769167 | RHO | c.840C>T (p.Gly280=)
| |
| 3 | g.129532677T>A | CA354470544 | RHO | c.841T>A (p.Ser281Thr)
| |
| 3 | g.129532677T>C | CA354470548 | RHO | c.841T>C (p.Ser281Pro)
| |
| 3 | g.129532677T>G | CA354470546 | RHO | c.841T>G (p.Ser281Ala)
| |
| 3 | g.129532678C>A | CA354470549 | RHO | c.842C>A (p.Ser281Tyr)
| |
| 3 | g.129532678C>G | CA354470552 | RHO | c.842C>G (p.Ser281Cys)
| |
| 3 | g.129532678C>T | CA354470551 | RHO | c.842C>T (p.Ser281Phe)
| gnomAD v4 |
| 3 | g.129532679C>A | CA435769170 | RHO | c.843C>A (p.Ser281=)
| |
| 3 | g.129532679C>G | CA435769172 | RHO | c.843C>G (p.Ser281=)
| |
| 3 | g.129532679C>T | CA435769173 | RHO | c.843C>T (p.Ser281=)
| |
| 3 | g.129532680A>C | CA354470554 | RHO | c.844A>C (p.Asn282His)
| |
| 3 | g.129532680A>G | CA354470557 | RHO | c.844A>G (p.Asn282Asp)
| |
| 3 | g.129532680A>T | CA354470556 | RHO | c.844A>T (p.Asn282Tyr)
| |
| 3 | g.129532681A>C | CA354470559 | RHO | c.845A>C (p.Asn282Thr)
| |
| 3 | g.129532681A>G | CA354470561 | RHO | c.845A>G (p.Asn282Ser)
| gnomAD v4 |
| 3 | g.129532681A>T | CA354470562 | RHO | c.845A>T (p.Asn282Ile)
| |
| 3 | g.129532682C>A | CA354470564 | RHO | c.846C>A (p.Asn282Lys)
| gnomAD v4 |
| 3 | g.129532682C= | CA1401211895 | RHO | c.846C= (p.Asn282=)
| |
| 3 | g.129532682C>G | CA354470565 | RHO | c.846C>G (p.Asn282Lys)
| |
| 3 | g.129532682C>T | CA435769176 | RHO | c.846C>T (p.Asn282=)
| ClinVar dbSNP |
| 3 | g.129532683T>A | CA354470567 | RHO | c.847T>A (p.Phe283Ile)
| |
| 3 | g.129532683T>C | CA354470569 | RHO | c.847T>C (p.Phe283Leu)
| ClinVar dbSNP |
| 3 | g.129532683T>G | CA354470571 | RHO | c.847T>G (p.Phe283Val)
| |
| 3 | g.129532683T= | CA1401211897 | RHO | c.847T= (p.Phe283=)
| |
| 3 | g.129532684T>A | CA354470572 | RHO | c.848T>A (p.Phe283Tyr)
| |
| 3 | g.129532684T>C | CA354470574 | RHO | c.848T>C (p.Phe283Ser)
| |
| 3 | g.129532684T>G | CA354470575 | RHO | c.848T>G (p.Phe283Cys)
| |
| 3 | g.129532685C>A | CA354470577 | RHO | c.849C>A (p.Phe283Leu)
| dbSNP |
| 3 | g.129532685C= | CA1401211900 | RHO | c.849C= (p.Phe283=)
| |
| 3 | g.129532685C>G | CA354470579 | RHO | c.849C>G (p.Phe283Leu)
| |
| 3 | g.129532685C>T | CA2607296 | RHO | c.849C>T (p.Phe283=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532686G>A | CA10604486 | RHO | c.850G>A (p.Gly284Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.129532686G>C | CA354470582 | RHO | c.850G>C (p.Gly284Arg)
| |
| 3 | g.129532686G= | CA1401211909 | RHO | c.850G= (p.Gly284=)
| |
| 3 | g.129532686G>T | CA2607297 | RHO | c.850G>T (p.Gly284Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.129532687G>A | CA354470585 | RHO | c.851G>A (p.Gly284Asp)
| ClinVar dbSNP gnomAD v4 |
| 3 | g.129532687G>C | CA354470586 | RHO | c.851G>C (p.Gly284Ala)
| |
| 3 | g.129532687G= | CA1401211919 | RHO | c.851G= (p.Gly284=)
| |
| 3 | g.129532687G>T | CA354470588 | RHO | c.851G>T (p.Gly284Val)
| dbSNP gnomAD v4 |
| 3 | g.129532688T>A | CA435769184 | RHO | c.852T>A (p.Gly284=)
| gnomAD v4 |
| 3 | g.129532688T>C | CA435769185 | RHO | c.852T>C (p.Gly284=)
| |
| 3 | g.129532688T>G | CA435769186 | RHO | c.852T>G (p.Gly284=)
| |
| 3 | g.129532689C>A | CA354470589 | RHO | c.853C>A (p.Pro285Thr)
| gnomAD v4 |
| 3 | g.129532689C= | CA1401211922 | RHO | c.853C= (p.Pro285=)
| |
| 3 | g.129532689C>G | CA82620799 | RHO | c.853C>G (p.Pro285Ala)
| dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.129532689C>T | CA354470592 | RHO | c.853C>T (p.Pro285Ser)
| |
| 3 | g.129532691dup | CA2667617511 | RHO | c.855dup (p.Ile286HisfsTer?)
| gnomAD v4 |
| 3 | g.129532690C>A | CA354470595 | RHO | c.854C>A (p.Pro285His)
| dbSNP gnomAD v4 |
| 3 | g.129532690C= | CA1401211926 | RHO | c.854C= (p.Pro285=)
| |
| 3 | g.129532690C>G | CA354470596 | RHO | c.854C>G (p.Pro285Arg)
| |
| 3 | g.129532690C>T | CA354470594 | RHO | c.854C>T (p.Pro285Leu)
| dbSNP |
| 3 | g.129532691C>A | CA435769190 | RHO | c.855C>A (p.Pro285=)
| |
| 3 | g.129532691C= | CA1401211931 | RHO | c.855C= (p.Pro285=)
| |
| 3 | g.129532691C>G | CA435769191 | RHO | c.855C>G (p.Pro285=)
| |
| 3 | g.129532691C>T | CA435769192 | RHO | c.855C>T (p.Pro285=)
| ClinVar dbSNP |
| 3 | g.129532692A>C | CA354470599 | RHO | c.856A>C (p.Ile286Leu)
| |
| 3 | g.129532692A>G | CA354470600 | RHO | c.856A>G (p.Ile286Val)
| ClinVar |
| 3 | g.129532692A>T | CA354470602 | RHO | c.856A>T (p.Ile286Phe)
| |
| 3 | g.129532693T>A | CA354470604 | RHO | c.857T>A (p.Ile286Asn)
| |
| 3 | g.129532693T>C | CA354470606 | RHO | c.857T>C (p.Ile286Thr)
| dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.129532693T>G | CA354470607 | RHO | c.857T>G (p.Ile286Ser)
| |
| 3 | g.129532693T= | CA1401211934 | RHO | c.857T= (p.Ile286=)
| |
| 3 | g.129532694C>A | CA435769194 | RHO | c.858C>A (p.Ile286=)
| |
| 3 | g.129532694C>G | CA354470609 | RHO | c.858C>G (p.Ile286Met)
| |
| 3 | g.129532694C>T | CA435769198 | RHO | c.858C>T (p.Ile286=)
| |
| 3 | g.129532695T>A | CA354470611 | RHO | c.859T>A (p.Phe287Ile)
| |
| 3 | g.129532695T>C | CA354470613 | RHO | c.859T>C (p.Phe287Leu)
| gnomAD v4 |
| 3 | g.129532695T>G | CA354470615 | RHO | c.859T>G (p.Phe287Val)
| COSMIC |
| 3 | g.129532696T>A | CA354470621 | RHO | c.860T>A (p.Phe287Tyr)
| |
| 3 | g.129532696T>C | CA354470623 | RHO | c.860T>C (p.Phe287Ser)
| |
| 3 | g.129532696T>G | CA354470626 | RHO | c.860T>G (p.Phe287Cys)
| |
| 3 | g.129532697C>A | CA354470629 | RHO | c.861C>A (p.Phe287Leu)
| |
| 3 | g.129532697C= | CA1401211938 | RHO | c.861C= (p.Phe287=)
| |
| 3 | g.129532697C>G | CA354470632 | RHO | c.861C>G (p.Phe287Leu)
| |
| 3 | g.129532697C>T | CA435769202 | RHO | c.861C>T (p.Phe287=)
| dbSNP |
| 3 | g.129532698A= | CA1401211942 | RHO | c.862A= (p.Met288=)
| |
| 3 | g.129532698A>C | CA354470635 | RHO | c.862A>C (p.Met288Leu)
| |
| 3 | g.129532698A>G | CA354470637 | RHO | c.862A>G (p.Met288Val)
| dbSNP |
| 3 | g.129532698A>T | CA354470640 | RHO | c.862A>T (p.Met288Leu)
| |
| 3 | g.129532699T>A | CA354470644 | RHO | c.863T>A (p.Met288Lys)
| |
| 3 | g.129532699T>C | CA354470645 | RHO | c.863T>C (p.Met288Thr)
| gnomAD v4 |
| 3 | g.129532699T>G | CA354470648 | RHO | c.863T>G (p.Met288Arg)
| gnomAD v4 |
| 3 | g.129532700G>A | CA354470652 | RHO | c.864G>A (p.Met288Ile)
| |
| 3 | g.129532700G>C | CA354470654 | RHO | c.864G>C (p.Met288Ile)
| |
| 3 | g.129532700G>T | CA354470656 | RHO | c.864G>T (p.Met288Ile)
| |
| 3 | g.129532701A= | CA1401211945 | RHO | c.865A= (p.Thr289=)
| |
| 3 | g.129532701A>C | CA354470659 | RHO | c.865A>C (p.Thr289Pro)
| ClinVar |
| 3 | g.129532701A>G | CA354470662 | RHO | c.865A>G (p.Thr289Ala)
| gnomAD v4 |
| 3 | g.129532701A>T | CA2607298 | RHO | c.865A>T (p.Thr289Ser)
| dbSNP ExAC gnomAD v2 |
| 3 | g.129532702C>A | CA354470668 | RHO | c.866C>A (p.Thr289Asn)
| |
| 3 | g.129532702C>G | CA354470671 | RHO | c.866C>G (p.Thr289Ser)
| gnomAD v4 |
| 3 | g.129532702C>T | CA354470665 | RHO | c.866C>T (p.Thr289Ile)
| |
| 3 | g.129532703C>A | CA435769207 | RHO | c.867C>A (p.Thr289=)
| |
| 3 | g.129532703C= | CA1401211949 | RHO | c.867C= (p.Thr289=)
| |
| 3 | g.129532703C>G | CA435769209 | RHO | c.867C>G (p.Thr289=)
| |
| 3 | g.129532703C>T | CA435769210 | RHO | c.867C>T (p.Thr289=)
| dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.129532704A>C | CA354470679 | RHO | c.868A>C (p.Ile290Leu)
| |
| 3 | g.129532704A>G | CA354470674 | RHO | c.868A>G (p.Ile290Val)
| |
| 3 | g.129532704A>T | CA354470676 | RHO | c.868A>T (p.Ile290Phe)
| |
| 3 | g.129532705T>A | CA354470681 | RHO | c.869T>A (p.Ile290Asn)
| ClinVar dbSNP gnomAD v4 |
| 3 | g.129532705T>C | CA2607299 | RHO | c.869T>C (p.Ile290Thr)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532705T>G | CA354470685 | RHO | c.869T>G (p.Ile290Ser)
| |
| 3 | g.129532705T= | CA1401211952 | RHO | c.869T= (p.Ile290=)
| |
| 3 | g.129532706C>A | CA435769211 | RHO | c.870C>A (p.Ile290=)
| |
| 3 | g.129532706C= | CA1401211955 | RHO | c.870C= (p.Ile290=)
| |
| 3 | g.129532706C>G | CA354470688 | RHO | c.870C>G (p.Ile290Met)
| |
| 3 | g.129532706C>T | CA2607300 | RHO | c.870C>T (p.Ile290=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532707C>A | CA354470693 | RHO | c.871C>A (p.Pro291Thr)
| |
| 3 | g.129532707C>G | CA354470695 | RHO | c.871C>G (p.Pro291Ala)
| |
| 3 | g.129532707C>T | CA354470698 | RHO | c.871C>T (p.Pro291Ser)
| |
| 3 | g.129532708C>A | CA354470702 | RHO | c.872C>A (p.Pro291Gln)
| |
| 3 | g.129532708C>G | CA354470705 | RHO | c.872C>G (p.Pro291Arg)
| |
| 3 | g.129532708C>T | CA354470707 | RHO | c.872C>T (p.Pro291Leu)
| |
| 3 | g.129532709A= | CA1401211961 | RHO | c.873A= (p.Pro291=)
| |
| 3 | g.129532709A>C | CA435769212 | RHO | c.873A>C (p.Pro291=)
| |
| 3 | g.129532709A>G | CA435769213 | RHO | c.873A>G (p.Pro291=)
| dbSNP |
| 3 | g.129532709A>T | CA435769214 | RHO | c.873A>T (p.Pro291=)
| |
| 3 | g.129532710G>A | CA354470715 | RHO | c.874G>A (p.Ala292Thr)
| dbSNP gnomAD v4 |
| 3 | g.129532710G>C | CA354470710 | RHO | c.874G>C (p.Ala292Pro)
| |
| 3 | g.129532710G= | CA1401211965 | RHO | c.874G= (p.Ala292=)
| |
| 3 | g.129532710G>T | CA354470713 | RHO | c.874G>T (p.Ala292Ser)
| |
| 3 | g.129532711C>A | CA122822 | RHO | c.875C>A (p.Ala292Glu)
| ClinVar dbSNP |
| 3 | g.129532711C= | CA1401211971 | RHO | c.875C= (p.Ala292=)
| |
| 3 | g.129532711C>G | CA354470719 | RHO | c.875C>G (p.Ala292Gly)
| |
| 3 | g.129532711C>T | CA354470722 | RHO | c.875C>T (p.Ala292Val)
| ClinVar dbSNP |
| 3 | g.129532712G>A | CA2607301 | RHO | c.876G>A (p.Ala292=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.129532712G>C | CA435769215 | RHO | c.876G>C (p.Ala292=)
| ClinVar dbSNP gnomAD v4 |
| 3 | g.129532712G= | CA1401211978 | RHO | c.876G= (p.Ala292=)
| |
| 3 | g.129532712G>T | CA435769216 | RHO | c.876G>T (p.Ala292=)
| |
| 3 | g.129532713T>A | CA354470726 | RHO | c.877T>A (p.Phe293Ile)
| |
| 3 | g.129532713T>C | CA354470728 | RHO | c.877T>C (p.Phe293Leu)
| |
| 3 | g.129532713T>G | CA354470731 | RHO | c.877T>G (p.Phe293Val)
| |
| 3 | g.129532714T>A | CA354470735 | RHO | c.878T>A (p.Phe293Tyr)
| |
| 3 | g.129532714T>C | CA354470736 | RHO | c.878T>C (p.Phe293Ser)
| |
| 3 | g.129532714T>G | CA354470739 | RHO | c.878T>G (p.Phe293Cys)
| |
| 3 | g.129532715C>A | CA354470743 | RHO | c.879C>A (p.Phe293Leu)
| |
| 3 | g.129532715C>G | CA354470745 | RHO | c.879C>G (p.Phe293Leu)
| |
| 3 | g.129532715C>T | CA435769217 | RHO | c.879C>T (p.Phe293=)
| COSMIC |
| 3 | g.129532716T>A | CA354470754 | RHO | c.880T>A (p.Phe294Ile)
| |
| 3 | g.129532716T>C | CA354470751 | RHO | c.880T>C (p.Phe294Leu)
| |
| 3 | g.129532716T>G | CA354470747 | RHO | c.880T>G (p.Phe294Val)
| |
| 3 | g.129532717T>A | CA354470757 | RHO | c.881T>A (p.Phe294Tyr)
| |
| 3 | g.129532717T>C | CA354470759 | RHO | c.881T>C (p.Phe294Ser)
| |
| 3 | g.129532717T>G | CA354470762 | RHO | c.881T>G (p.Phe294Cys)
| |
| 3 | g.129532718T>A | CA354470764 | RHO | c.882T>A (p.Phe294Leu)
| |
| 3 | g.129532718T>C | CA435769218 | RHO | c.882T>C (p.Phe294=)
| |
| 3 | g.129532718T>G | CA354470766 | RHO | c.882T>G (p.Phe294Leu)
| |
| 3 | g.129532719G>A | CA354470776 | RHO | c.883G>A (p.Ala295Thr)
| gnomAD v4 |
| 3 | g.129532719G>C | CA354470772 | RHO | c.883G>C (p.Ala295Pro)
| |
| 3 | g.129532719G>T | CA354470771 | RHO | c.883G>T (p.Ala295Ser)
| |
| 3 | g.129532720C>A | CA354470780 | RHO | c.884C>A (p.Ala295Asp)
| |
| 3 | g.129532720C>G | CA354470782 | RHO | c.884C>G (p.Ala295Gly)
| |
| 3 | g.129532720C>T | CA354470783 | RHO | c.884C>T (p.Ala295Val)
| |
| 3 | g.129532721C>A | CA435769219 | RHO | c.885C>A (p.Ala295=)
| |
| 3 | g.129532721C>G | CA435769220 | RHO | c.885C>G (p.Ala295=)
| |
| 3 | g.129532721C>T | CA435769221 | RHO | c.885C>T (p.Ala295=)
| |
| 3 | g.129532722A= | CA1401211987 | RHO | c.886A= (p.Lys296=)
| |
| 3 | g.129532722A>C | CA354470787 | RHO | c.886A>C (p.Lys296Gln)
| ClinVar dbSNP |
| 3 | g.129532722A>G | CA256677 | RHO | c.886A>G (p.Lys296Glu)
| ClinVar dbSNP |
| 3 | g.129532722A>T | CA354470792 | RHO | c.886A>T (p.Lys296Ter)
| |
| 3 | g.129532723A>C | CA354470793 | RHO | c.887A>C (p.Lys296Thr)
| |
| 3 | g.129532723A>G | CA354470798 | RHO | c.887A>G (p.Lys296Arg)
| |
| 3 | g.129532723A>T | CA354470795 | RHO | c.887A>T (p.Lys296Met)
| |
| 3 | g.129532724G>A | CA435769222 | RHO | c.888G>A (p.Lys296=)
| ClinVar gnomAD v4 |
| 3 | g.129532724G>C | CA354470800 | RHO | c.888G>C (p.Lys296Asn)
| ClinVar dbSNP |
| 3 | g.129532724G= | CA1401211995 | RHO | c.888G= (p.Lys296=)
| |
| 3 | g.129532724G>T | CA354470802 | RHO | c.888G>T (p.Lys296Asn)
| ClinVar |
| 3 | g.129532725A>C | CA354470804 | RHO | c.889A>C (p.Ser297Arg)
| ClinVar |
| 3 | g.129532725A>G | CA354470806 | RHO | c.889A>G (p.Ser297Gly)
| |
| 3 | g.129532725A>T | CA354470808 | RHO | c.889A>T (p.Ser297Cys)
| |
| 3 | g.129532726G>A | CA354470810 | RHO | c.890G>A (p.Ser297Asn)
| |
| 3 | g.129532726G>C | CA354470812 | RHO | c.890G>C (p.Ser297Thr)
| |
| 3 | g.129532726G>T | CA354470815 | RHO | c.890G>T (p.Ser297Ile)
| |
| 3 | g.129532727C>A | CA354470817 | RHO | c.891C>A (p.Ser297Arg)
| |
| 3 | g.129532727C= | CA1401212009 | RHO | c.891C= (p.Ser297=)
| |
| 3 | g.129532727C>G | CA354470820 | RHO | c.891C>G (p.Ser297Arg)
| ClinVar dbSNP |
| 3 | g.129532727C>T | CA232817 | RHO | c.891C>T (p.Ser297=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532728G>A | CA2607302 | RHO | c.892G>A (p.Ala298Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.129532728G>C | CA354470829 | RHO | c.892G>C (p.Ala298Pro)
| |
| 3 | g.129532728G= | CA1401212016 | RHO | c.892G= (p.Ala298=)
| |
| 3 | g.129532728G>T | CA354470827 | RHO | c.892G>T (p.Ala298Ser)
| dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.129532729C>A | CA354470834 | RHO | c.893C>A (p.Ala298Asp)
| dbSNP |
| 3 | g.129532729C= | CA1401212023 | RHO | c.893C= (p.Ala298=)
| |
| 3 | g.129532729C>G | CA354470839 | RHO | c.893C>G (p.Ala298Gly)
| COSMIC |
| 3 | g.129532729C>T | CA354470836 | RHO | c.893C>T (p.Ala298Val)
| ClinVar |
| 3 | g.129532730C>A | CA435769223 | RHO | c.894C>A (p.Ala298=)
| |
| 3 | g.129532730C= | CA1401212027 | RHO | c.894C= (p.Ala298=)
| |
| 3 | g.129532730C>G | CA2607304 | RHO | c.894C>G (p.Ala298=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.129532730C>T | CA2607303 | RHO | c.894C>T (p.Ala298=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532731G>A | CA2607306 | RHO | c.895G>A (p.Ala299Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532731G>C | CA354470847 | RHO | c.895G>C (p.Ala299Pro)
| |
| 3 | g.129532731G= | CA1401212032 | RHO | c.895G= (p.Ala299=)
| |
| 3 | g.129532731G>T | CA2607305 | RHO | c.895G>T (p.Ala299Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.129532732C>A | CA354470851 | RHO | c.896C>A (p.Ala299Asp)
| |
| 3 | g.129532732C>G | CA354470854 | RHO | c.896C>G (p.Ala299Gly)
| |
| 3 | g.129532732C>T | CA354470856 | RHO | c.896C>T (p.Ala299Val)
| |
| 3 | g.129532733C>A | CA435769224 | RHO | c.897C>A (p.Ala299=)
| |
| 3 | g.129532733C= | CA1401212038 | RHO | c.897C= (p.Ala299=)
| |
| 3 | g.129532733C>G | CA435769225 | RHO | c.897C>G (p.Ala299=)
| |
| 3 | g.129532733C>T | CA435769226 | RHO | c.897C>T (p.Ala299=)
| dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.129532734A= | CA1401212046 | RHO | c.898A= (p.Ile300=)
| |
| 3 | g.129532734A>C | CA354470859 | RHO | c.898A>C (p.Ile300Leu)
| |
| 3 | g.129532734A>G | CA354470862 | RHO | c.898A>G (p.Ile300Val)
| |
| 3 | g.129532734A>T | CA2607307 | RHO | c.898A>T (p.Ile300Phe)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.129532735T>A | CA354470867 | RHO | c.899T>A (p.Ile300Asn)
| |
| 3 | g.129532735T>C | CA354470870 | RHO | c.899T>C (p.Ile300Thr)
| |
| 3 | g.129532735T>G | CA354470872 | RHO | c.899T>G (p.Ile300Ser)
| |
| 3 | g.129532736C>A | CA435769227 | RHO | c.900C>A (p.Ile300=)
| gnomAD v4 |
| 3 | g.129532736C>G | CA354470875 | RHO | c.900C>G (p.Ile300Met)
| |
| 3 | g.129532736C>T | CA435769228 | RHO | c.900C>T (p.Ile300=)
| |
