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 |
6 | g.79921715T>A | CA364656633 | ELOVL4 | c.451A>T (p.Asn151Tyr)
| |
6 | g.79921715T>C | CA364656634 | ELOVL4 | c.451A>G (p.Asn151Asp)
| |
6 | g.79921715T>G | CA364656635 | ELOVL4 | c.451A>C (p.Asn151His)
| |
6 | g.79921716T>A | CA364656636 | ELOVL4 | c.450A>T (p.Lys150Asn)
| |
6 | g.79921716T>C | CA451068532 | ELOVL4 | c.450A>G (p.Lys150=)
| |
6 | g.79921716T>G | CA364656637 | ELOVL4 | c.450A>C (p.Lys150Asn)
| |
6 | g.79921717T>A | CA364656638 | ELOVL4 | c.449A>T (p.Lys150Ile)
| |
6 | g.79921717T>C | CA364656639 | ELOVL4 | c.449A>G (p.Lys150Arg)
| |
6 | g.79921717T>G | CA364656640 | ELOVL4 | c.449A>C (p.Lys150Thr)
| |
6 | g.79921718T>A | CA364656641 | ELOVL4 | c.448A>T (p.Lys150Ter)
| |
6 | g.79921718T>C | CA364656642 | ELOVL4 | c.448A>G (p.Lys150Glu)
| |
6 | g.79921718T>G | CA364656643 | ELOVL4 | c.448A>C (p.Lys150Gln)
| |
6 | g.79921719C>A | CA364656645 | ELOVL4 | c.447G>T (p.Lys149Asn)
| |
6 | g.79921719C>G | CA364656644 | ELOVL4 | c.447G>C (p.Lys149Asn)
| |
6 | g.79921719C>T | CA451068533 | ELOVL4 | c.447G>A (p.Lys149=)
| gnomAD v4 |
6 | g.79921720T>A | CA364656646 | ELOVL4 | c.446A>T (p.Lys149Met)
| |
6 | g.79921720T>C | CA364656648 | ELOVL4 | c.446A>G (p.Lys149Arg)
| ClinVar dbSNP gnomAD v4 COSMIC |
6 | g.79921720T>G | CA364656647 | ELOVL4 | c.446A>C (p.Lys149Thr)
| |
6 | g.79921721T>A | CA364656649 | ELOVL4 | c.445A>T (p.Lys149Ter)
| |
6 | g.79921721T>C | CA364656651 | ELOVL4 | c.445A>G (p.Lys149Glu)
| |
6 | g.79921721T>G | CA364656650 | ELOVL4 | c.445A>C (p.Lys149Gln)
| |
6 | g.79921722T>A | CA364656652 | ELOVL4 | c.444A>T (p.Arg148Ser)
| |
6 | g.79921722T>C | CA451068534 | ELOVL4 | c.444A>G (p.Arg148=)
| COSMIC |
6 | g.79921722T>G | CA364656653 | ELOVL4 | c.444A>C (p.Arg148Ser)
| |
6 | g.79921723C>A | CA364656654 | ELOVL4 | c.443G>T (p.Arg148Ile)
| ClinVar dbSNP |
6 | g.79921723C= | CA1640824987 | ELOVL4 | c.443G= (p.Arg148=)
| |
6 | g.79921723C>G | CA364656655 | ELOVL4 | c.443G>C (p.Arg148Thr)
| |
6 | g.79921723C>T | CA364656656 | ELOVL4 | c.443G>A (p.Arg148Lys)
| |
6 | g.79921724T>A | CA364656657 | ELOVL4 | c.442A>T (p.Arg148Ter)
| |
6 | g.79921724T>C | CA364656658 | ELOVL4 | c.442A>G (p.Arg148Gly)
| |
6 | g.79921724T>G | CA451068535 | ELOVL4 | c.442A>C (p.Arg148=)
| |
6 | g.79921725C>A | CA451068536 | ELOVL4 | c.441G>T (p.Leu147=)
| |
6 | g.79921725C>G | CA451068538 | ELOVL4 | c.441G>C (p.Leu147=)
| |
6 | g.79921725C>T | CA451068537 | ELOVL4 | c.441G>A (p.Leu147=)
| gnomAD v4 |
6 | g.79921726A>C | CA364656659 | ELOVL4 | c.440T>G (p.Leu147Arg)
| |
6 | g.79921726A>G | CA364656660 | ELOVL4 | c.440T>C (p.Leu147Pro)
| |
6 | g.79921726A>T | CA364656661 | ELOVL4 | c.440T>A (p.Leu147Gln)
| |
6 | g.79921727G>A | CA451068539 | ELOVL4 | c.439C>T (p.Leu147=)
| |
6 | g.79921727G>C | CA364656662 | ELOVL4 | c.439C>G (p.Leu147Val)
| |
6 | g.79921727G= | CA1640824988 | ELOVL4 | c.439C= (p.Leu147=)
| |
6 | g.79921727G>T | CA364656663 | ELOVL4 | c.439C>A (p.Leu147Met)
| dbSNP |
6 | g.79921728A= | CA1640824989 | ELOVL4 | c.438T= (p.Ile146=)
| |
6 | g.79921728A>C | CA364656664 | ELOVL4 | c.438T>G (p.Ile146Met)
| |
6 | g.79921728A>G | CA451068540 | ELOVL4 | c.438T>C (p.Ile146=)
| dbSNP gnomAD v4 |
6 | g.79921728A>T | CA451068541 | ELOVL4 | c.438T>A (p.Ile146=)
| |
6 | g.79921729A>C | CA364656667 | ELOVL4 | c.437T>G (p.Ile146Ser)
| |
6 | g.79921729A>G | CA364656665 | ELOVL4 | c.437T>C (p.Ile146Thr)
| |
6 | g.79921729A>T | CA364656666 | ELOVL4 | c.437T>A (p.Ile146Asn)
| |
6 | g.79921730T>A | CA364656668 | ELOVL4 | c.436A>T (p.Ile146Phe)
| |
6 | g.79921730T>C | CA364656669 | ELOVL4 | c.436A>G (p.Ile146Val)
| |
6 | g.79921730T>G | CA364656670 | ELOVL4 | c.436A>C (p.Ile146Leu)
| |
6 | g.79921730dup | CA2573141259 | ELOVL4 | c.436dup (p.Ile146AsnfsTer29)
| ClinVar dbSNP |
6 | g.79921730_79921731delinsTA | CA1640824990 | ELOVL4 | c.435_436delinsTA (p.Phe145=)
| |
6 | g.79921731A>C | CA364656671 | ELOVL4 | c.435T>G (p.Phe145Leu)
| |
6 | g.79921731A>G | CA451068542 | ELOVL4 | c.435T>C (p.Phe145=)
| |
6 | g.79921731A>T | CA364656672 | ELOVL4 | c.435T>A (p.Phe145Leu)
| |
6 | g.79921736dup | CA1640824991 | ELOVL4 | c.435dup (p.Ile146TyrfsTer29)
| ClinVar dbSNP |
6 | g.79921736del | CA3901534 | ELOVL4 | c.435del (p.Phe145LeufsTer3)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921732A>C | CA364656673 | ELOVL4 | c.434T>G (p.Phe145Cys)
| |
6 | g.79921732A>G | CA364656674 | ELOVL4 | c.434T>C (p.Phe145Ser)
| |
6 | g.79921732A>T | CA364656675 | ELOVL4 | c.434T>A (p.Phe145Tyr)
| |
6 | g.79921733A>C | CA364656676 | ELOVL4 | c.433T>G (p.Phe145Val)
| |
6 | g.79921733A>G | CA364656677 | ELOVL4 | c.433T>C (p.Phe145Leu)
| |
6 | g.79921733A>T | CA364656678 | ELOVL4 | c.433T>A (p.Phe145Ile)
| |
6 | g.79921734A>C | CA364656680 | ELOVL4 | c.432T>G (p.Phe144Leu)
| |
6 | g.79921734A>G | CA451068543 | ELOVL4 | c.432T>C (p.Phe144=)
| |
6 | g.79921734A>T | CA364656679 | ELOVL4 | c.432T>A (p.Phe144Leu)
| |
6 | g.79921735A= | CA1640824992 | ELOVL4 | c.431T= (p.Phe144=)
| |
6 | g.79921735A>C | CA142271132 | ELOVL4 | c.431T>G (p.Phe144Cys)
| dbSNP gnomAD v4 |
6 | g.79921735A>G | CA364656681 | ELOVL4 | c.431T>C (p.Phe144Ser)
| |
6 | g.79921735A>T | CA364656682 | ELOVL4 | c.431T>A (p.Phe144Tyr)
| |
6 | g.79921736A>C | CA364656683 | ELOVL4 | c.430T>G (p.Phe144Val)
| |
6 | g.79921736A>G | CA364656684 | ELOVL4 | c.430T>C (p.Phe144Leu)
| |
6 | g.79921736A>T | CA364656685 | ELOVL4 | c.430T>A (p.Phe144Ile)
| |
6 | g.79921737C>A | CA451068544 | ELOVL4 | c.429G>T (p.Val143=)
| |
6 | g.79921737C= | CA1640824993 | ELOVL4 | c.429G= (p.Val143=)
| |
6 | g.79921737C>G | CA451068545 | ELOVL4 | c.429G>C (p.Val143=)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921737C>T | CA142271133 | ELOVL4 | c.429G>A (p.Val143=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921738A= | CA1640824994 | ELOVL4 | c.428T= (p.Val143=)
| |
6 | g.79921738A>C | CA364656686 | ELOVL4 | c.428T>G (p.Val143Gly)
| |
6 | g.79921738A>G | CA364656687 | ELOVL4 | c.428T>C (p.Val143Ala)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.79921738A>T | CA364656688 | ELOVL4 | c.428T>A (p.Val143Glu)
| |
6 | g.79921739C>A | CA364656689 | ELOVL4 | c.427G>T (p.Val143Leu)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
6 | g.79921739C= | CA1640824996 | ELOVL4 | c.427G= (p.Val143=)
| |
6 | g.79921739C>G | CA364656690 | ELOVL4 | c.427G>C (p.Val143Leu)
| |
6 | g.79921739C>T | CA364656691 | ELOVL4 | c.427G>A (p.Val143Met)
| dbSNP |
6 | g.79921739_79921741delinsCTG | CA1640824995 | ELOVL4 | c.425_427delinsCAG (p.Thr142=)
| |
6 | g.79921740T>A | CA451068547 | ELOVL4 | c.426A>T (p.Thr142=)
| |
6 | g.79921740T>C | CA3901535 | ELOVL4 | c.426A>G (p.Thr142=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921740T>G | CA451068546 | ELOVL4 | c.426A>C (p.Thr142=)
| |
6 | g.79921740T= | CA1640824997 | ELOVL4 | c.426A= (p.Thr142=)
| |
6 | g.79921743_79921744del | CA568600871 | ELOVL4 | c.425_426del (p.Thr142SerfsTer?)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921741G>A | CA364656694 | ELOVL4 | c.425C>T (p.Thr142Ile)
| |
6 | g.79921741G>C | CA364656693 | ELOVL4 | c.425C>G (p.Thr142Arg)
| |
6 | g.79921741G>T | CA364656692 | ELOVL4 | c.425C>A (p.Thr142Lys)
| |
6 | g.79921742T>A | CA364656695 | ELOVL4 | c.424A>T (p.Thr142Ser)
| |
6 | g.79921742T>C | CA364656696 | ELOVL4 | c.424A>G (p.Thr142Ala)
| |
6 | g.79921742T>G | CA364656697 | ELOVL4 | c.424A>C (p.Thr142Pro)
| |
6 | g.79921743G>A | CA451068548 | ELOVL4 | c.423C>T (p.Asp141=)
| dbSNP |
6 | g.79921743G>C | CA364656698 | ELOVL4 | c.423C>G (p.Asp141Glu)
| |
6 | g.79921743G= | CA1640824998 | ELOVL4 | c.423C= (p.Asp141=)
| |
6 | g.79921743G>T | CA364656699 | ELOVL4 | c.423C>A (p.Asp141Glu)
| |
6 | g.79921744T>A | CA364656700 | ELOVL4 | c.422A>T (p.Asp141Val)
| |
6 | g.79921744T>C | CA364656701 | ELOVL4 | c.422A>G (p.Asp141Gly)
| |
6 | g.79921744T>G | CA364656702 | ELOVL4 | c.422A>C (p.Asp141Ala)
| |
6 | g.79921745C>A | CA364656703 | ELOVL4 | c.421G>T (p.Asp141Tyr)
| |
6 | g.79921745C>G | CA364656704 | ELOVL4 | c.421G>C (p.Asp141His)
| |
6 | g.79921745C>T | CA364656705 | ELOVL4 | c.421G>A (p.Asp141Asn)
| |
6 | g.79921746C>A | CA364656706 | ELOVL4 | c.420G>T (p.Leu140Phe)
| |
6 | g.79921746C= | CA1640824999 | ELOVL4 | c.420G= (p.Leu140=)
| |
6 | g.79921746C>G | CA364656707 | ELOVL4 | c.420G>C (p.Leu140Phe)
| |
6 | g.79921746C>T | CA3901536 | ELOVL4 | c.420G>A (p.Leu140=)
| dbSNP ExAC gnomAD v2 |
6 | g.79921747A>C | CA364656709 | ELOVL4 | c.419T>G (p.Leu140Trp)
| |
6 | g.79921747A>G | CA364656710 | ELOVL4 | c.419T>C (p.Leu140Ser)
| |
6 | g.79921747A>T | CA364656708 | ELOVL4 | c.419T>A (p.Leu140Ter)
| |
6 | g.79921748A>C | CA364656711 | ELOVL4 | c.418T>G (p.Leu140Val)
| |
6 | g.79921748A>G | CA451068549 | ELOVL4 | c.418T>C (p.Leu140=)
| |
6 | g.79921748A>T | CA364656712 | ELOVL4 | c.418T>A (p.Leu140Met)
| |
6 | g.79921749A>C | CA364656713 | ELOVL4 | c.417T>G (p.Tyr139Ter)
| |
6 | g.79921749A>G | CA451068550 | ELOVL4 | c.417T>C (p.Tyr139=)
| |
6 | g.79921749A>T | CA364656714 | ELOVL4 | c.417T>A (p.Tyr139Ter)
| |
6 | g.79921750T>A | CA364656715 | ELOVL4 | c.416A>T (p.Tyr139Phe)
| |
6 | g.79921750T>C | CA364656716 | ELOVL4 | c.416A>G (p.Tyr139Cys)
| |
6 | g.79921750T>G | CA364656717 | ELOVL4 | c.416A>C (p.Tyr139Ser)
| |
6 | g.79921751A>C | CA364656718 | ELOVL4 | c.415T>G (p.Tyr139Asp)
| |
6 | g.79921751A>G | CA364656719 | ELOVL4 | c.415T>C (p.Tyr139His)
| |
6 | g.79921751A>T | CA364656720 | ELOVL4 | c.415T>A (p.Tyr139Asn)
| |
6 | g.79921752C>A | CA364656721 | ELOVL4 | c.414G>T (p.Glu138Asp)
| ClinVar |
6 | g.79921752C>G | CA364656722 | ELOVL4 | c.414G>C (p.Glu138Asp)
| |
6 | g.79921752C>T | CA451068551 | ELOVL4 | c.414G>A (p.Glu138=)
| |
6 | g.79921752_79921754del | CA2679489860 | ELOVL4 | c.412_414del (p.Glu138del)
| gnomAD v4 |
6 | g.79921753T>A | CA364656723 | ELOVL4 | c.413A>T (p.Glu138Val)
| |
6 | g.79921753T>C | CA364656724 | ELOVL4 | c.413A>G (p.Glu138Gly)
| |
6 | g.79921753T>G | CA364656725 | ELOVL4 | c.413A>C (p.Glu138Ala)
| |
6 | g.79921753_79921755del | CA2771859721 | ELOVL4 | c.411_413del (p.Glu138del)
| |
6 | g.79921754C>A | CA364656728 | ELOVL4 | c.412G>T (p.Glu138Ter)
| |
6 | g.79921754C>G | CA364656726 | ELOVL4 | c.412G>C (p.Glu138Gln)
| |
6 | g.79921754C>T | CA364656727 | ELOVL4 | c.412G>A (p.Glu138Lys)
| |
6 | g.79921755A>C | CA451068552 | ELOVL4 | c.411T>G (p.Val137=)
| |
6 | g.79921755A>G | CA451068553 | ELOVL4 | c.411T>C (p.Val137=)
| |
6 | g.79921755A>T | CA451068554 | ELOVL4 | c.411T>A (p.Val137=)
| |
6 | g.79921756del | CA2771859722 | ELOVL4 | c.411del (p.Glu138SerfsTer10)
| |
6 | g.79921756A>C | CA364656729 | ELOVL4 | c.410T>G (p.Val137Gly)
| |
6 | g.79921756A>G | CA364656730 | ELOVL4 | c.410T>C (p.Val137Ala)
| |
6 | g.79921756A>T | CA364656731 | ELOVL4 | c.410T>A (p.Val137Asp)
| |
6 | g.79921757C>A | CA364656732 | ELOVL4 | c.409G>T (p.Val137Phe)
| |
6 | g.79921757C>G | CA364656733 | ELOVL4 | c.409G>C (p.Val137Leu)
| |
6 | g.79921757C>T | CA364656734 | ELOVL4 | c.409G>A (p.Val137Ile)
| ClinVar dbSNP gnomAD v4 |
6 | g.79921758T>A | CA451068555 | ELOVL4 | c.408A>T (p.Gly136=)
| |
6 | g.79921758T>C | CA451068556 | ELOVL4 | c.408A>G (p.Gly136=)
| gnomAD v4 |
6 | g.79921758T>G | CA451068557 | ELOVL4 | c.408A>C (p.Gly136=)
| |
6 | g.79921758_79921775del | CA2771859723 | ELOVL4 | c.391_408del (p.Tyr131_Gly136del)
| |
6 | g.79921759C>A | CA364656735 | ELOVL4 | c.407G>T (p.Gly136Val)
| |
6 | g.79921759C>G | CA364656736 | ELOVL4 | c.407G>C (p.Gly136Ala)
| |
6 | g.79921759C>T | CA364656737 | ELOVL4 | c.407G>A (p.Gly136Glu)
| |
6 | g.79921760C>A | CA364656738 | ELOVL4 | c.406G>T (p.Gly136Ter)
| |
6 | g.79921760C>G | CA364656739 | ELOVL4 | c.406G>C (p.Gly136Arg)
| |
6 | g.79921760C>T | CA364656740 | ELOVL4 | c.406G>A (p.Gly136Arg)
| |
6 | g.79921761T>A | CA364656741 | ELOVL4 | c.405A>T (p.Lys135Asn)
| |
6 | g.79921761T>C | CA451068558 | ELOVL4 | c.405A>G (p.Lys135=)
| ClinVar |
6 | g.79921761T>G | CA364656742 | ELOVL4 | c.405A>C (p.Lys135Asn)
| |
6 | g.79921762T>A | CA364656743 | ELOVL4 | c.404A>T (p.Lys135Ile)
| |
6 | g.79921762T>C | CA364656744 | ELOVL4 | c.404A>G (p.Lys135Arg)
| |
6 | g.79921762T>G | CA364656745 | ELOVL4 | c.404A>C (p.Lys135Thr)
| |
6 | g.79921763T>A | CA364656746 | ELOVL4 | c.403A>T (p.Lys135Ter)
| |
6 | g.79921763T>C | CA364656747 | ELOVL4 | c.403A>G (p.Lys135Glu)
| |
6 | g.79921763T>G | CA364656748 | ELOVL4 | c.403A>C (p.Lys135Gln)
| |
6 | g.79921764A>C | CA451068559 | ELOVL4 | c.402T>G (p.Ser134=)
| |
6 | g.79921764A>G | CA451068561 | ELOVL4 | c.402T>C (p.Ser134=)
| |
6 | g.79921764A>T | CA451068560 | ELOVL4 | c.402T>A (p.Ser134=)
| |