6 | g.79921614A= | CA1640824954 | ELOVL4 | c.541+11T= (n.541+11T=)
| |
6 | g.79921614A>G | CA2771859718 | ELOVL4 | c.541+11T>C (n.541+11T>C)
| |
6 | g.79921615A= | CA1640824955 | ELOVL4 | c.541+10T= (n.541+10T=)
| |
6 | g.79921615A>T | CA1090954888 | ELOVL4 | c.541+10T>A (n.541+10T>A)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.79921615_79921616insTA | CA142271126 | ELOVL4 | c.541+10_541+11insAT (n.541+10_541+11insAT)
| dbSNP |
6 | g.79921616A= | CA1640824956 | ELOVL4 | c.541+9T= (n.541+9T=)
| |
6 | g.79921616A>T | CA142271127 | ELOVL4 | c.541+9T>A (n.541+9T>A)
| dbSNP |
6 | g.79921618T>G | CA3901521 | ELOVL4 | c.541+7A>C (n.541+7A>C)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921618T= | CA1640824957 | ELOVL4 | c.541+7A= (n.541+7A=)
| |
6 | g.79921619G= | CA1640824958 | ELOVL4 | c.541+6C= (n.541+6C=)
| |
6 | g.79921619G>T | CA3901522 | ELOVL4 | c.541+6C>A (n.541+6C>A)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921620C>T | CA2578677066 | ELOVL4 | c.541+5G>A (n.541+5G>A)
| ClinVar |
6 | g.79921623A>C | CA364656419 | ELOVL4 | c.541+2T>G (n.541+2T>G)
| gnomAD v4 |
6 | g.79921623A>G | CA364656420 | ELOVL4 | c.541+2T>C (n.541+2T>C)
| |
6 | g.79921623A>T | CA364656421 | ELOVL4 | c.541+2T>A (n.541+2T>A)
| |
6 | g.79921624C>A | CA364656422 | ELOVL4 | c.541+1G>T (n.541+1G>T)
| |
6 | g.79921624C>G | CA364656423 | ELOVL4 | c.541+1G>C (n.541+1G>C)
| |
6 | g.79921624C>T | CA364656424 | ELOVL4 | c.541+1G>A (n.541+1G>A)
| |
6 | g.79921625C>A | CA364656427 | ELOVL4 | c.541G>T (p.Ala181Ser)
| |
6 | g.79921625C>G | CA364656425 | ELOVL4 | c.541G>C (p.Ala181Pro)
| |
6 | g.79921625C>T | CA364656426 | ELOVL4 | c.541G>A (p.Ala181Thr)
| |
6 | g.79921626T>A | CA364656428 | ELOVL4 | c.540A>T (p.Gln180His)
| |
6 | g.79921626T>C | CA3901523 | ELOVL4 | c.540A>G (p.Gln180=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921626T>G | CA364656429 | ELOVL4 | c.540A>C (p.Gln180His)
| |
6 | g.79921626T= | CA1640824959 | ELOVL4 | c.540A= (p.Gln180=)
| |
6 | g.79921627T>A | CA364656430 | ELOVL4 | c.539A>T (p.Gln180Leu)
| |
6 | g.79921627T>C | CA364656431 | ELOVL4 | c.539A>G (p.Gln180Arg)
| |
6 | g.79921627T>G | CA364656432 | ELOVL4 | c.539A>C (p.Gln180Pro)
| ClinVar dbSNP |
6 | g.79921628_79921629del | CA2531281113 | ELOVL4 | c.538_539del (p.Gln180SerfsTer?)
| |
6 | g.79921628G>A | CA364656433 | ELOVL4 | c.538C>T (p.Gln180Ter)
| |
6 | g.79921628G>C | CA364656434 | ELOVL4 | c.538C>G (p.Gln180Glu)
| |
6 | g.79921628G>T | CA364656435 | ELOVL4 | c.538C>A (p.Gln180Lys)
| |
6 | g.79921629T>A | CA451068487 | ELOVL4 | c.537A>T (p.Gly179=)
| |
6 | g.79921629T>C | CA3901524 | ELOVL4 | c.537A>G (p.Gly179=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921629T>G | CA451068488 | ELOVL4 | c.537A>C (p.Gly179=)
| |
6 | g.79921629T= | CA1640824960 | ELOVL4 | c.537A= (p.Gly179=)
| |
6 | g.79921630C>A | CA364656436 | ELOVL4 | c.536G>T (p.Gly179Val)
| |
6 | g.79921630C>G | CA364656437 | ELOVL4 | c.536G>C (p.Gly179Ala)
| |
6 | g.79921630C>T | CA364656438 | ELOVL4 | c.536G>A (p.Gly179Glu)
| |
6 | g.79921631C>A | CA364656441 | ELOVL4 | c.535G>T (p.Gly179Ter)
| gnomAD v4 |
6 | g.79921631C>G | CA364656439 | ELOVL4 | c.535G>C (p.Gly179Arg)
| |
6 | g.79921631C>T | CA364656440 | ELOVL4 | c.535G>A (p.Gly179Arg)
| |
6 | g.79921632T>A | CA451068490 | ELOVL4 | c.534A>T (p.Gly178=)
| |
6 | g.79921632T>C | CA451068491 | ELOVL4 | c.534A>G (p.Gly178=)
| |
6 | g.79921632T>G | CA451068492 | ELOVL4 | c.534A>C (p.Gly178=)
| |
6 | g.79921633C>A | CA364656442 | ELOVL4 | c.533G>T (p.Gly178Val)
| |
6 | g.79921633C>G | CA364656443 | ELOVL4 | c.533G>C (p.Gly178Ala)
| |
6 | g.79921633C>T | CA364656444 | ELOVL4 | c.533G>A (p.Gly178Glu)
| |
6 | g.79921634C>A | CA364656445 | ELOVL4 | c.532G>T (p.Gly178Ter)
| gnomAD v4 |
6 | g.79921634C>G | CA364656446 | ELOVL4 | c.532G>C (p.Gly178Arg)
| |
6 | g.79921634C>T | CA364656447 | ELOVL4 | c.532G>A (p.Gly178Arg)
| |
6 | g.79921635T>A | CA451068493 | ELOVL4 | c.531A>T (p.Ala177=)
| |
6 | g.79921635T>C | CA451068495 | ELOVL4 | c.531A>G (p.Ala177=)
| |
6 | g.79921635T>G | CA451068494 | ELOVL4 | c.531A>C (p.Ala177=)
| |
6 | g.79921636G>A | CA364656450 | ELOVL4 | c.530C>T (p.Ala177Val)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921636G>C | CA364656449 | ELOVL4 | c.530C>G (p.Ala177Gly)
| |
6 | g.79921636G= | CA1640824961 | ELOVL4 | c.530C= (p.Ala177=)
| |
6 | g.79921636G>T | CA364656448 | ELOVL4 | c.530C>A (p.Ala177Glu)
| |
6 | g.79921637C>A | CA364656451 | ELOVL4 | c.529G>T (p.Ala177Ser)
| gnomAD v4 |
6 | g.79921637C>G | CA364656452 | ELOVL4 | c.529G>C (p.Ala177Pro)
| |
6 | g.79921637C>T | CA364656453 | ELOVL4 | c.529G>A (p.Ala177Thr)
| COSMIC |
6 | g.79921638A>C | CA451068497 | ELOVL4 | c.528T>G (p.Val176=)
| |
6 | g.79921638A>G | CA451068498 | ELOVL4 | c.528T>C (p.Val176=)
| |
6 | g.79921638A>T | CA451068499 | ELOVL4 | c.528T>A (p.Val176=)
| |
6 | g.79921639A>C | CA364656454 | ELOVL4 | c.527T>G (p.Val176Gly)
| |
6 | g.79921639A>G | CA364656455 | ELOVL4 | c.527T>C (p.Val176Ala)
| |
6 | g.79921639A>T | CA364656456 | ELOVL4 | c.527T>A (p.Val176Asp)
| |
6 | g.79921640C>A | CA364656457 | ELOVL4 | c.526G>T (p.Val176Phe)
| |
6 | g.79921640C>G | CA364656459 | ELOVL4 | c.526G>C (p.Val176Leu)
| COSMIC |
6 | g.79921640C>T | CA364656458 | ELOVL4 | c.526G>A (p.Val176Ile)
| |
6 | g.79921641C>A | CA364656460 | ELOVL4 | c.525G>T (p.Trp175Cys)
| gnomAD v4 |
6 | g.79921641C>G | CA364656461 | ELOVL4 | c.525G>C (p.Trp175Cys)
| |
6 | g.79921641C>T | CA364656462 | ELOVL4 | c.525G>A (p.Trp175Ter)
| |
6 | g.79921642C>A | CA364656463 | ELOVL4 | c.524G>T (p.Trp175Leu)
| |
6 | g.79921642C>G | CA364656464 | ELOVL4 | c.524G>C (p.Trp175Ser)
| |
6 | g.79921642C>T | CA364656465 | ELOVL4 | c.524G>A (p.Trp175Ter)
| |
6 | g.79921643A= | CA1640824962 | ELOVL4 | c.523T= (p.Trp175=)
| |
6 | g.79921643A>C | CA364656466 | ELOVL4 | c.523T>G (p.Trp175Gly)
| |
6 | g.79921643A>G | CA3901525 | ELOVL4 | c.523T>C (p.Trp175Arg)
| dbSNP ExAC gnomAD v2 |
6 | g.79921643A>T | CA364656467 | ELOVL4 | c.523T>A (p.Trp175Arg)
| |
6 | g.79921644C>A | CA364656468 | ELOVL4 | c.522G>T (p.Lys174Asn)
| |
6 | g.79921644C= | CA1640824963 | ELOVL4 | c.522G= (p.Lys174=)
| |
6 | g.79921644C>G | CA142271128 | ELOVL4 | c.522G>C (p.Lys174Asn)
| dbSNP |
6 | g.79921644C>T | CA451068500 | ELOVL4 | c.522G>A (p.Lys174=)
| gnomAD v4 |
6 | g.79921645T>A | CA364656469 | ELOVL4 | c.521A>T (p.Lys174Met)
| |
6 | g.79921645T>C | CA364656471 | ELOVL4 | c.521A>G (p.Lys174Arg)
| |
6 | g.79921645T>G | CA364656470 | ELOVL4 | c.521A>C (p.Lys174Thr)
| |
6 | g.79921646T>A | CA364656472 | ELOVL4 | c.520A>T (p.Lys174Ter)
| |
6 | g.79921646T>C | CA364656474 | ELOVL4 | c.520A>G (p.Lys174Glu)
| |
6 | g.79921646T>G | CA364656473 | ELOVL4 | c.520A>C (p.Lys174Gln)
| |
6 | g.79921647A>C | CA364656475 | ELOVL4 | c.519T>G (p.Ile173Met)
| |
6 | g.79921647A>G | CA451068501 | ELOVL4 | c.519T>C (p.Ile173=)
| |
6 | g.79921647A>T | CA451068502 | ELOVL4 | c.519T>A (p.Ile173=)
| |
6 | g.79921648A>C | CA364656476 | ELOVL4 | c.518T>G (p.Ile173Ser)
| |
6 | g.79921648A>G | CA364656477 | ELOVL4 | c.518T>C (p.Ile173Thr)
| |
6 | g.79921648A>T | CA364656478 | ELOVL4 | c.518T>A (p.Ile173Asn)
| |
6 | g.79921649T>A | CA364656479 | ELOVL4 | c.517A>T (p.Ile173Phe)
| |
6 | g.79921649T>C | CA364656480 | ELOVL4 | c.517A>G (p.Ile173Val)
| |
6 | g.79921649T>G | CA364656481 | ELOVL4 | c.517A>C (p.Ile173Leu)
| |
6 | g.79921650T>A | CA451068503 | ELOVL4 | c.516A>T (p.Gly172=)
| |
6 | g.79921650T>C | CA451068504 | ELOVL4 | c.516A>G (p.Gly172=)
| |
6 | g.79921650T>G | CA451068505 | ELOVL4 | c.516A>C (p.Gly172=)
| |
6 | g.79921651C>A | CA364656482 | ELOVL4 | c.515G>T (p.Gly172Val)
| COSMIC |
6 | g.79921651C>G | CA364656483 | ELOVL4 | c.515G>C (p.Gly172Ala)
| |
6 | g.79921651C>T | CA364656484 | ELOVL4 | c.515G>A (p.Gly172Glu)
| |
6 | g.79921652del | CA2679489853 | ELOVL4 | c.515del (p.Gly172GlufsTer16)
| gnomAD v4 |
6 | g.79921652C>A | CA364656485 | ELOVL4 | c.514G>T (p.Gly172Ter)
| |
6 | g.79921652C>G | CA364656486 | ELOVL4 | c.514G>C (p.Gly172Arg)
| |
6 | g.79921652C>T | CA364656487 | ELOVL4 | c.514G>A (p.Gly172Arg)
| |
6 | g.79921653A>C | CA364656488 | ELOVL4 | c.513T>G (p.Ile171Met)
| |
6 | g.79921653A>G | CA451068506 | ELOVL4 | c.513T>C (p.Ile171=)
| |
6 | g.79921653A>T | CA451068507 | ELOVL4 | c.513T>A (p.Ile171=)
| |
6 | g.79921654A= | CA1640824964 | ELOVL4 | c.512T= (p.Ile171=)
| |
6 | g.79921654A>C | CA364656489 | ELOVL4 | c.512T>G (p.Ile171Ser)
| |
6 | g.79921654A>G | CA364656490 | ELOVL4 | c.512T>C (p.Ile171Thr)
| ClinVar dbSNP |
6 | g.79921654A>T | CA364656491 | ELOVL4 | c.512T>A (p.Ile171Asn)
| |
6 | g.79921655T>A | CA364656492 | ELOVL4 | c.511A>T (p.Ile171Phe)
| |
6 | g.79921655T>C | CA364656493 | ELOVL4 | c.511A>G (p.Ile171Val)
| gnomAD v4 |
6 | g.79921655T>G | CA364656494 | ELOVL4 | c.511A>C (p.Ile171Leu)
| |
6 | g.79921656C>A | CA364656495 | ELOVL4 | c.510G>T (p.Trp170Cys)
| |
6 | g.79921656C>G | CA364656496 | ELOVL4 | c.510G>C (p.Trp170Cys)
| COSMIC |
6 | g.79921656C>T | CA364656497 | ELOVL4 | c.510G>A (p.Trp170Ter)
| |
6 | g.79921657C>A | CA364656498 | ELOVL4 | c.509G>T (p.Trp170Leu)
| |
6 | g.79921657C= | CA1640824965 | ELOVL4 | c.509G= (p.Trp170=)
| |
6 | g.79921657C>G | CA364656499 | ELOVL4 | c.509G>C (p.Trp170Ser)
| |
6 | g.79921657C>T | CA364656500 | ELOVL4 | c.509G>A (p.Trp170Ter)
| |
6 | g.79921657_79921658insTTAATT | CA568600870 | ELOVL4 | c.508_509insAATTAA (p.Trp170Ter)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921658A>C | CA364656503 | ELOVL4 | c.508T>G (p.Trp170Gly)
| |
6 | g.79921658A>G | CA364656502 | ELOVL4 | c.508T>C (p.Trp170Arg)
| |
6 | g.79921658A>T | CA364656501 | ELOVL4 | c.508T>A (p.Trp170Arg)
| |
6 | g.79921659C>A | CA364656504 | ELOVL4 | c.507G>T (p.Trp169Cys)
| COSMIC |
6 | g.79921659C>G | CA364656505 | ELOVL4 | c.507G>C (p.Trp169Cys)
| |
6 | g.79921659C>T | CA364656506 | ELOVL4 | c.507G>A (p.Trp169Ter)
| |
6 | g.79921660C>A | CA364656507 | ELOVL4 | c.506G>T (p.Trp169Leu)
| |
6 | g.79921660C= | CA1640824966 | ELOVL4 | c.506G= (p.Trp169=)
| |
6 | g.79921660C>G | CA364656508 | ELOVL4 | c.506G>C (p.Trp169Ser)
| |
6 | g.79921660C>T | CA16605161 | ELOVL4 | c.506G>A (p.Trp169Ter)
| ClinVar dbSNP |
6 | g.79921661A>C | CA364656511 | ELOVL4 | c.505T>G (p.Trp169Gly)
| |
6 | g.79921661A>G | CA364656509 | ELOVL4 | c.505T>C (p.Trp169Arg)
| |
6 | g.79921661A>T | CA364656510 | ELOVL4 | c.505T>A (p.Trp169Arg)
| |
6 | g.79921662C>A | CA364656512 | ELOVL4 | c.504G>T (p.Leu168Phe)
| |
6 | g.79921662C= | CA1640824967 | ELOVL4 | c.504G= (p.Leu168=)
| |
6 | g.79921662C>G | CA170078 | ELOVL4 | c.504G>C (p.Leu168Phe)
| ClinVar dbSNP |
6 | g.79921662C>T | CA142271129 | ELOVL4 | c.504G>A (p.Leu168=)
| dbSNP gnomAD v4 |
6 | g.79921663A>C | CA364656513 | ELOVL4 | c.503T>G (p.Leu168Trp)
| |
6 | g.79921663A>G | CA364656514 | ELOVL4 | c.503T>C (p.Leu168Ser)
| |
6 | g.79921663A>T | CA364656515 | ELOVL4 | c.503T>A (p.Leu168Ter)
| |
6 | g.79921664A= | CA1640824968 | ELOVL4 | c.502T= (p.Leu168=)
| |
6 | g.79921664A>C | CA364656516 | ELOVL4 | c.502T>G (p.Leu168Val)
| |
6 | g.79921664A>G | CA10627695 | ELOVL4 | c.502T>C (p.Leu168=)
| ClinVar dbSNP gnomAD v4 |
6 | g.79921664A>T | CA364656517 | ELOVL4 | c.502T>A (p.Leu168Met)
| |
6 | g.79921665G>A | CA451068508 | ELOVL4 | c.501C>T (p.Thr167=)
| COSMIC |
6 | g.79921665G>C | CA451068510 | ELOVL4 | c.501C>G (p.Thr167=)
| |
6 | g.79921665G>T | CA451068509 | ELOVL4 | c.501C>A (p.Thr167=)
| |
6 | g.79921666G>A | CA364656518 | ELOVL4 | c.500C>T (p.Thr167Ile)
| |
6 | g.79921666G>C | CA364656519 | ELOVL4 | c.500C>G (p.Thr167Ser)
| |
6 | g.79921666G>T | CA364656520 | ELOVL4 | c.500C>A (p.Thr167Asn)
| |
6 | g.79921667T>A | CA364656521 | ELOVL4 | c.499A>T (p.Thr167Ser)
| |
6 | g.79921667T>C | CA364656522 | ELOVL4 | c.499A>G (p.Thr167Ala)
| |
6 | g.79921667T>G | CA364656523 | ELOVL4 | c.499A>C (p.Thr167Pro)
| gnomAD v4 |
6 | g.79921668A>C | CA364656524 | ELOVL4 | c.498T>G (p.Phe166Leu)
| |
6 | g.79921668A>G | CA451068511 | ELOVL4 | c.498T>C (p.Phe166=)
| |
6 | g.79921668A>T | CA364656525 | ELOVL4 | c.498T>A (p.Phe166Leu)
| |
6 | g.79921669A>C | CA364656526 | ELOVL4 | c.497T>G (p.Phe166Cys)
| |
6 | g.79921669A>G | CA364656527 | ELOVL4 | c.497T>C (p.Phe166Ser)
| |
6 | g.79921669A>T | CA364656528 | ELOVL4 | c.497T>A (p.Phe166Tyr)
| |
6 | g.79921670A= | CA1640824969 | ELOVL4 | c.496T= (p.Phe166=)
| |
6 | g.79921670A>C | CA364656529 | ELOVL4 | c.496T>G (p.Phe166Val)
| dbSNP gnomAD v2 |
6 | g.79921670A>G | CA364656531 | ELOVL4 | c.496T>C (p.Phe166Leu)
| |
6 | g.79921670A>T | CA364656530 | ELOVL4 | c.496T>A (p.Phe166Ile)
| |
6 | g.79921671C>A | CA364656532 | ELOVL4 | c.495G>T (p.Met165Ile)
| |
6 | g.79921671C= | CA1640824970 | ELOVL4 | c.495G= (p.Met165=)
| |
6 | g.79921671C>G | CA364656534 | ELOVL4 | c.495G>C (p.Met165Ile)
| |
6 | g.79921671C>T | CA364656533 | ELOVL4 | c.495G>A (p.Met165Ile)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.79921672A>C | CA364656535 | ELOVL4 | c.494T>G (p.Met165Arg)
| |
6 | g.79921672A>G | CA364656536 | ELOVL4 | c.494T>C (p.Met165Thr)
| |
6 | g.79921672A>T | CA364656537 | ELOVL4 | c.494T>A (p.Met165Lys)
| |
6 | g.79921673T>A | CA364656538 | ELOVL4 | c.493A>T (p.Met165Leu)
| |
6 | g.79921673T>C | CA364656539 | ELOVL4 | c.493A>G (p.Met165Val)
| gnomAD v4 |
6 | g.79921673T>G | CA364656540 | ELOVL4 | c.493A>C (p.Met165Leu)
| |
6 | g.79921674C>A | CA451068512 | ELOVL4 | c.492G>T (p.Thr164=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.79921674C= | CA1640824971 | ELOVL4 | c.492G= (p.Thr164=)
| |
6 | g.79921674C>G | CA451068513 | ELOVL4 | c.492G>C (p.Thr164=)
| dbSNP |
6 | g.79921674C>T | CA142271130 | ELOVL4 | c.492G>A (p.Thr164=)
| ClinVar dbSNP gnomAD v4 |
6 | g.79921675G>A | CA3901526 | ELOVL4 | c.491C>T (p.Thr164Met)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921675G>C | CA364656541 | ELOVL4 | c.491C>G (p.Thr164Arg)
| |
6 | g.79921675G= | CA1640824972 | ELOVL4 | c.491C= (p.Thr164=)
| |
6 | g.79921675G>T | CA364656542 | ELOVL4 | c.491C>A (p.Thr164Lys)
| |
6 | g.79921676T>A | CA364656543 | ELOVL4 | c.490A>T (p.Thr164Ser)
| |
6 | g.79921676T>C | CA142271131 | ELOVL4 | c.490A>G (p.Thr164Ala)
| dbSNP |
6 | g.79921676T>G | CA364656544 | ELOVL4 | c.490A>C (p.Thr164Pro)
| |
6 | g.79921676T= | CA1640824973 | ELOVL4 | c.490A= (p.Thr164=)
| |
6 | g.79921677A= | CA1640824974 | ELOVL4 | c.489T= (p.Cys163=)
| |
6 | g.79921677A>C | CA364656546 | ELOVL4 | c.489T>G (p.Cys163Trp)
| |
6 | g.79921677A>G | CA3901527 | ELOVL4 | c.489T>C (p.Cys163=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921677A>T | CA364656545 | ELOVL4 | c.489T>A (p.Cys163Ter)
| |
6 | g.79921678_79921679del | CA2679489855 | ELOVL4 | c.488_489del (p.Cys163TyrfsTer11)
| gnomAD v4 |
6 | g.79921678C>A | CA364656547 | ELOVL4 | c.488G>T (p.Cys163Phe)
| |
6 | g.79921678C= | CA1640824975 | ELOVL4 | c.488G= (p.Cys163=)
| |
6 | g.79921678C>G | CA364656548 | ELOVL4 | c.488G>C (p.Cys163Ser)
| |
6 | g.79921678C>T | CA3901528 | ELOVL4 | c.488G>A (p.Cys163Tyr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921679A= | CA1640824976 | ELOVL4 | c.487T= (p.Cys163=)
| |
6 | g.79921679A>C | CA364656549 | ELOVL4 | c.487T>G (p.Cys163Gly)
| dbSNP |
6 | g.79921679A>G | CA364656550 | ELOVL4 | c.487T>C (p.Cys163Arg)
| |
6 | g.79921679A>T | CA3901529 | ELOVL4 | c.487T>A (p.Cys163Ser)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921680G>A | CA3901530 | ELOVL4 | c.486C>T (p.His162=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921680G>C | CA364656551 | ELOVL4 | c.486C>G (p.His162Gln)
| |
6 | g.79921680G= | CA1640824977 | ELOVL4 | c.486C= (p.His162=)
| |
6 | g.79921680G>T | CA364656552 | ELOVL4 | c.486C>A (p.His162Gln)
| |
6 | g.79921681T>A | CA364656553 | ELOVL4 | c.485A>T (p.His162Leu)
| |
6 | g.79921681T>C | CA364656554 | ELOVL4 | c.485A>G (p.His162Arg)
| |
6 | g.79921681T>G | CA364656555 | ELOVL4 | c.485A>C (p.His162Pro)
| |
6 | g.79921682G>A | CA364656556 | ELOVL4 | c.484C>T (p.His162Tyr)
| |
6 | g.79921682G>C | CA364656558 | ELOVL4 | c.484C>G (p.His162Asp)
| |
6 | g.79921682G>T | CA364656557 | ELOVL4 | c.484C>A (p.His162Asn)
| |
6 | g.79921683A>C | CA364656559 | ELOVL4 | c.483T>G (p.His161Gln)
| |
6 | g.79921683A>G | CA451068514 | ELOVL4 | c.483T>C (p.His161=)
| |
6 | g.79921683A>T | CA364656560 | ELOVL4 | c.483T>A (p.His161Gln)
| |
6 | g.79921684T>A | CA364656561 | ELOVL4 | c.482A>T (p.His161Leu)
| |
6 | g.79921684T>C | CA364656562 | ELOVL4 | c.482A>G (p.His161Arg)
| ClinVar |
6 | g.79921684T>G | CA364656563 | ELOVL4 | c.482A>C (p.His161Pro)
| |
6 | g.79921685G>A | CA364656564 | ELOVL4 | c.481C>T (p.His161Tyr)
| |
6 | g.79921685G>C | CA364656565 | ELOVL4 | c.481C>G (p.His161Asp)
| |
6 | g.79921685G>T | CA364656566 | ELOVL4 | c.481C>A (p.His161Asn)
| |
6 | g.79921686A>C | CA364656567 | ELOVL4 | c.480T>G (p.Tyr160Ter)
| |
6 | g.79921686A>G | CA451068515 | ELOVL4 | c.480T>C (p.Tyr160=)
| |
6 | g.79921686A>T | CA364656568 | ELOVL4 | c.480T>A (p.Tyr160Ter)
| |
6 | g.79921687T>A | CA364656571 | ELOVL4 | c.479A>T (p.Tyr160Phe)
| |
6 | g.79921687T>C | CA364656570 | ELOVL4 | c.479A>G (p.Tyr160Cys)
| gnomAD v4 |
6 | g.79921687T>G | CA364656569 | ELOVL4 | c.479A>C (p.Tyr160Ser)
| |
6 | g.79921688A>C | CA364656572 | ELOVL4 | c.478T>G (p.Tyr160Asp)
| |
6 | g.79921688A>G | CA364656573 | ELOVL4 | c.478T>C (p.Tyr160His)
| |
6 | g.79921688A>T | CA364656574 | ELOVL4 | c.478T>A (p.Tyr160Asn)
| |
6 | g.79921689C>A | CA451068516 | ELOVL4 | c.477G>T (p.Val159=)
| |
6 | g.79921689C>G | CA451068517 | ELOVL4 | c.477G>C (p.Val159=)
| |
6 | g.79921689C>T | CA451068518 | ELOVL4 | c.477G>A (p.Val159=)
| |
6 | g.79921690A>C | CA364656575 | ELOVL4 | c.476T>G (p.Val159Gly)
| |
6 | g.79921690A>G | CA364656576 | ELOVL4 | c.476T>C (p.Val159Ala)
| |
6 | g.79921690A>T | CA364656577 | ELOVL4 | c.476T>A (p.Val159Glu)
| |
6 | g.79921691C>A | CA364656578 | ELOVL4 | c.475G>T (p.Val159Leu)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921691C= | CA1640824978 | ELOVL4 | c.475G= (p.Val159=)
| |
6 | g.79921691C>G | CA364656579 | ELOVL4 | c.475G>C (p.Val159Leu)
| |
6 | g.79921691C>T | CA364656580 | ELOVL4 | c.475G>A (p.Val159Met)
| ClinVar |
6 | g.79921692A= | CA1640824979 | ELOVL4 | c.474T= (p.His158=)
| |
6 | g.79921692A>C | CA364656581 | ELOVL4 | c.474T>G (p.His158Gln)
| |
6 | g.79921692A>G | CA3901531 | ELOVL4 | c.474T>C (p.His158=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921692A>T | CA364656582 | ELOVL4 | c.474T>A (p.His158Gln)
| gnomAD v4 |
6 | g.79921693T>A | CA364656583 | ELOVL4 | c.473A>T (p.His158Leu)
| |
6 | g.79921693T>C | CA364656584 | ELOVL4 | c.473A>G (p.His158Arg)
| ClinVar dbSNP |
6 | g.79921693T>G | CA3901532 | ELOVL4 | c.473A>C (p.His158Pro)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921693T= | CA1640824980 | ELOVL4 | c.473A= (p.His158=)
| |
6 | g.79921694G>A | CA364656587 | ELOVL4 | c.472C>T (p.His158Tyr)
| |
6 | g.79921694G>C | CA364656585 | ELOVL4 | c.472C>G (p.His158Asp)
| |
6 | g.79921694G>T | CA364656586 | ELOVL4 | c.472C>A (p.His158Asn)
| |
6 | g.79921697_79921700del | CA2771859720 | ELOVL4 | c.469_472del (p.Leu157MetfsTer30)
| |
6 | g.79921695A>C | CA451068519 | ELOVL4 | c.471T>G (p.Leu157=)
| |
6 | g.79921695A>G | CA451068520 | ELOVL4 | c.471T>C (p.Leu157=)
| |
6 | g.79921695A>T | CA451068521 | ELOVL4 | c.471T>A (p.Leu157=)
| |
6 | g.79921696A>C | CA364656588 | ELOVL4 | c.470T>G (p.Leu157Arg)
| |
6 | g.79921696A>G | CA364656589 | ELOVL4 | c.470T>C (p.Leu157Pro)
| |
6 | g.79921696A>T | CA364656590 | ELOVL4 | c.470T>A (p.Leu157His)
| |
6 | g.79921697G>A | CA364656591 | ELOVL4 | c.469C>T (p.Leu157Phe)
| |
6 | g.79921697G>C | CA364656592 | ELOVL4 | c.469C>G (p.Leu157Val)
| |
6 | g.79921697G>T | CA364656593 | ELOVL4 | c.469C>A (p.Leu157Ile)
| |
6 | g.79921698G>A | CA451068522 | ELOVL4 | c.468C>T (p.Phe156=)
| |
6 | g.79921698G>C | CA364656594 | ELOVL4 | c.468C>G (p.Phe156Leu)
| |
6 | g.79921698G= | CA1640824981 | ELOVL4 | c.468C= (p.Phe156=)
| |
6 | g.79921698G>T | CA3901533 | ELOVL4 | c.468C>A (p.Phe156Leu)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921699A= | CA1640824982 | ELOVL4 | c.467T= (p.Phe156=)
| |
6 | g.79921699A>C | CA364656595 | ELOVL4 | c.467T>G (p.Phe156Cys)
| |
6 | g.79921699A>G | CA233951 | ELOVL4 | c.467T>C (p.Phe156Ser)
| ClinVar dbSNP gnomAD v4 |
6 | g.79921699A>T | CA364656596 | ELOVL4 | c.467T>A (p.Phe156Tyr)
| |
6 | g.79921700A>C | CA364656599 | ELOVL4 | c.466T>G (p.Phe156Val)
| gnomAD v4 |
6 | g.79921700A>G | CA364656597 | ELOVL4 | c.466T>C (p.Phe156Leu)
| |
6 | g.79921700A>T | CA364656598 | ELOVL4 | c.466T>A (p.Phe156Ile)
| |
6 | g.79921701A>C | CA451068525 | ELOVL4 | c.465T>G (p.Ser155=)
| |
6 | g.79921701A>G | CA451068524 | ELOVL4 | c.465T>C (p.Ser155=)
| |
6 | g.79921701A>T | CA451068523 | ELOVL4 | c.465T>A (p.Ser155=)
| |
6 | g.79921702G>A | CA364656600 | ELOVL4 | c.464C>T (p.Ser155Phe)
| COSMIC |
6 | g.79921702G>C | CA364656601 | ELOVL4 | c.464C>G (p.Ser155Cys)
| |
6 | g.79921702G>T | CA364656602 | ELOVL4 | c.464C>A (p.Ser155Tyr)
| gnomAD v4 |
6 | g.79921703A>C | CA364656603 | ELOVL4 | c.463T>G (p.Ser155Ala)
| |
6 | g.79921703A>G | CA364656604 | ELOVL4 | c.463T>C (p.Ser155Pro)
| gnomAD v4 |
6 | g.79921703A>T | CA364656605 | ELOVL4 | c.463T>A (p.Ser155Thr)
| |
6 | g.79921704A>C | CA451068526 | ELOVL4 | c.462T>G (p.Val154=)
| |
6 | g.79921704A>G | CA451068528 | ELOVL4 | c.462T>C (p.Val154=)
| |
6 | g.79921704A>T | CA451068527 | ELOVL4 | c.462T>A (p.Val154=)
| |
6 | g.79921705A>C | CA364656606 | ELOVL4 | c.461T>G (p.Val154Gly)
| |
6 | g.79921705A>G | CA364656607 | ELOVL4 | c.461T>C (p.Val154Ala)
| |
6 | g.79921705A>T | CA364656608 | ELOVL4 | c.461T>A (p.Val154Asp)
| |
6 | g.79921706C>A | CA364656609 | ELOVL4 | c.460G>T (p.Val154Phe)
| |
6 | g.79921706C= | CA1640824983 | ELOVL4 | c.460G= (p.Val154=)
| |
6 | g.79921706C>G | CA364656610 | ELOVL4 | c.460G>C (p.Val154Leu)
| dbSNP |
6 | g.79921706C>T | CA364656611 | ELOVL4 | c.460G>A (p.Val154Ile)
| |
6 | g.79921707T>A | CA364656613 | ELOVL4 | c.459A>T (p.Gln153His)
| |
6 | g.79921707T>C | CA451068529 | ELOVL4 | c.459A>G (p.Gln153=)
| gnomAD v4 |
6 | g.79921707T>G | CA364656612 | ELOVL4 | c.459A>C (p.Gln153His)
| |
6 | g.79921708T>A | CA364656614 | ELOVL4 | c.458A>T (p.Gln153Leu)
| |
6 | g.79921708T>C | CA364656615 | ELOVL4 | c.458A>G (p.Gln153Arg)
| gnomAD v4 |
6 | g.79921708T>G | CA364656616 | ELOVL4 | c.458A>C (p.Gln153Pro)
| |
6 | g.79921709G>A | CA364656617 | ELOVL4 | c.457C>T (p.Gln153Ter)
| |
6 | g.79921709G>C | CA364656618 | ELOVL4 | c.457C>G (p.Gln153Glu)
| |
6 | g.79921709G= | CA1640824984 | ELOVL4 | c.457C= (p.Gln153=)
| |
6 | g.79921709G>T | CA364656619 | ELOVL4 | c.457C>A (p.Gln153Lys)
| |
6 | g.79921709_79921710insCGTTTAATTGCATATATGT | CA1640824985 | ELOVL4 | c.456_457insACATATATGCAATTAAACG (p.Gln153ThrfsTer28)
| dbSNP |
6 | g.79921710G>A | CA451068530 | ELOVL4 | c.456C>T (p.Asn152=)
| |
6 | g.79921710G>C | CA364656620 | ELOVL4 | c.456C>G (p.Asn152Lys)
| |
6 | g.79921710G>T | CA364656621 | ELOVL4 | c.456C>A (p.Asn152Lys)
| |
6 | g.79921711T>A | CA364656622 | ELOVL4 | c.455A>T (p.Asn152Ile)
| |
6 | g.79921711T>C | CA364656623 | ELOVL4 | c.455A>G (p.Asn152Ser)
| gnomAD v4 |
6 | g.79921711T>G | CA364656624 | ELOVL4 | c.455A>C (p.Asn152Thr)
| |
6 | g.79921712T>A | CA364656625 | ELOVL4 | c.454A>T (p.Asn152Tyr)
| |
6 | g.79921712T>C | CA364656626 | ELOVL4 | c.454A>G (p.Asn152Asp)
| |
6 | g.79921712T>G | CA364656627 | ELOVL4 | c.454A>C (p.Asn152His)
| gnomAD v4 |
6 | g.79921713G>A | CA451068531 | ELOVL4 | c.453C>T (p.Asn151=)
| dbSNP gnomAD v4 |
6 | g.79921713G>C | CA364656629 | ELOVL4 | c.453C>G (p.Asn151Lys)
| |
6 | g.79921713G= | CA1640824986 | ELOVL4 | c.453C= (p.Asn151=)
| |
6 | g.79921713G>T | CA364656628 | ELOVL4 | c.453C>A (p.Asn151Lys)
| |
6 | g.79921714T>A | CA364656630 | ELOVL4 | c.452A>T (p.Asn151Ile)
| |
6 | g.79921714T>C | CA364656631 | ELOVL4 | c.452A>G (p.Asn151Ser)
| gnomAD v4 |
6 | g.79921714T>G | CA364656632 | ELOVL4 | c.452A>C (p.Asn151Thr)
| |
6 | g.79921717_79921718del | CA2679489857 | ELOVL4 | c.451_452del (p.Asn151GlnfsTer23)
| gnomAD v4 |