6 | g.79921566T>C | CA828566425 | ELOVL4 | c.541+59A>G (n.541+59A>G)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.79921566T= | CA1640824929 | ELOVL4 | c.541+59A= (n.541+59A=)
| |
6 | g.79921568T>C | CA828566426 | ELOVL4 | c.541+57A>G (n.541+57A>G)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.79921568T= | CA1640824930 | ELOVL4 | c.541+57A= (n.541+57A=)
| |
6 | g.79921569C= | CA1640824931 | ELOVL4 | c.541+56G= (n.541+56G=)
| |
6 | g.79921569C>G | CA2679489797 | ELOVL4 | c.541+56G>C (n.541+56G>C)
| gnomAD v4 |
6 | g.79921569C>T | CA142271124 | ELOVL4 | c.541+56G>A (n.541+56G>A)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921570C>T | CA2578677065 | ELOVL4 | c.541+55G>A (n.541+55G>A)
| gnomAD v4 |
6 | g.79921573_79921579dup | CA2679489799 | ELOVL4 | c.541+49_541+55dup (n.541+49_541+55dup)
| gnomAD v4 |
6 | g.79921571A>T | CA2679489802 | ELOVL4 | c.541+54T>A (n.541+54T>A)
| gnomAD v4 |
6 | g.79921574G>T | CA2679489804 | ELOVL4 | c.541+51C>A (n.541+51C>A)
| gnomAD v4 |
6 | g.79921579_79921580dup | CA2679489805 | ELOVL4 | c.541+48_541+49dup (n.541+48_541+49dup)
| gnomAD v4 |
6 | g.79921577C>T | CA2679489807 | ELOVL4 | c.541+48G>A (n.541+48G>A)
| gnomAD v4 |
6 | g.79921579C>A | CA1090954876 | ELOVL4 | c.541+46G>T (n.541+46G>T)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.79921579C= | CA1640824932 | ELOVL4 | c.541+46G= (n.541+46G=)
| |
6 | g.79921580A= | CA1640824933 | ELOVL4 | c.541+45T= (n.541+45T=)
| |
6 | g.79921580A>G | CA828566427 | ELOVL4 | c.541+45T>C (n.541+45T>C)
| dbSNP |
6 | g.79921580A>T | CA2679489811 | ELOVL4 | c.541+45T>A (n.541+45T>A)
| gnomAD v4 |
6 | g.79921581T>A | CA1640824935 | ELOVL4 | c.541+44A>T (n.541+44A>T)
| dbSNP |
6 | g.79921581T>C | CA142271125 | ELOVL4 | c.541+44A>G (n.541+44A>G)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921581T= | CA1640824934 | ELOVL4 | c.541+44A= (n.541+44A=)
| |
6 | g.79921583T>C | CA3901510 | ELOVL4 | c.541+42A>G (n.541+42A>G)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921583T= | CA1640824936 | ELOVL4 | c.541+42A= (n.541+42A=)
| |
6 | g.79921584A= | CA1640824937 | ELOVL4 | c.541+41T= (n.541+41T=)
| |
6 | g.79921584A>G | CA3901511 | ELOVL4 | c.541+41T>C (n.541+41T>C)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921585T>C | CA568392513 | ELOVL4 | c.541+40A>G (n.541+40A>G)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921585T>G | CA2771859715 | ELOVL4 | c.541+40A>C (n.541+40A>C)
| |
6 | g.79921585T= | CA1640824938 | ELOVL4 | c.541+40A= (n.541+40A=)
| |
6 | g.79921586G>A | CA2679489820 | ELOVL4 | c.541+39C>T (n.541+39C>T)
| gnomAD v4 |
6 | g.79921586G>T | CA2679489822 | ELOVL4 | c.541+39C>A (n.541+39C>A)
| gnomAD v4 |
6 | g.79921587C>T | CA2679489825 | ELOVL4 | c.541+38G>A (n.541+38G>A)
| gnomAD v4 |
6 | g.79921588A>C | CA2712185257 | ELOVL4 | c.541+37T>G (n.541+37T>G)
| dbSNP |
6 | g.79921589A= | CA1640824939 | ELOVL4 | c.541+36T= (n.541+36T=)
| |
6 | g.79921589A>G | CA3901512 | ELOVL4 | c.541+36T>C (n.541+36T>C)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921590T>C | CA3901513 | ELOVL4 | c.541+35A>G (n.541+35A>G)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921590T>G | CA1640824941 | ELOVL4 | c.541+35A>C (n.541+35A>C)
| dbSNP |
6 | g.79921590T= | CA1640824940 | ELOVL4 | c.541+35A= (n.541+35A=)
| |
6 | g.79921591T>A | CA3901514 | ELOVL4 | c.541+34A>T (n.541+34A>T)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921591T>C | CA2711961261 | ELOVL4 | c.541+34A>G (n.541+34A>G)
| dbSNP |
6 | g.79921591T= | CA1640824942 | ELOVL4 | c.541+34A= (n.541+34A=)
| |
6 | g.79921595C= | CA1640824943 | ELOVL4 | c.541+30G= (n.541+30G=)
| |
6 | g.79921595C>T | CA3901515 | ELOVL4 | c.541+30G>A (n.541+30G>A)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921596G>A | CA3901516 | ELOVL4 | c.541+29C>T (n.541+29C>T)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921596G= | CA1640824944 | ELOVL4 | c.541+29C= (n.541+29C=)
| |
6 | g.79921596G>T | CA2679489834 | ELOVL4 | c.541+29C>A (n.541+29C>A)
| gnomAD v4 |
6 | g.79921598A= | CA1640824945 | ELOVL4 | c.541+27T= (n.541+27T=)
| |
6 | g.79921598A>G | CA1640824946 | ELOVL4 | c.541+27T>C (n.541+27T>C)
| dbSNP |
6 | g.79921599del | CA2679489836 | ELOVL4 | c.541+27del (n.541+27del)
| gnomAD v4 |
6 | g.79921600G>T | CA2679489837 | ELOVL4 | c.541+25C>A (n.541+25C>A)
| gnomAD v4 |
6 | g.79921601C>T | CA2679489838 | ELOVL4 | c.541+24G>A (n.541+24G>A)
| gnomAD v4 |
6 | g.79921603G>A | CA3901517 | ELOVL4 | c.541+22C>T (n.541+22C>T)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921603G>C | CA2679489839 | ELOVL4 | c.541+22C>G (n.541+22C>G)
| gnomAD v4 |
6 | g.79921603G= | CA1640824947 | ELOVL4 | c.541+22C= (n.541+22C=)
| |
6 | g.79921604T>C | CA650553869 | ELOVL4 | c.541+21A>G (n.541+21A>G)
| COSMIC |
6 | g.79921605A= | CA1640824949 | ELOVL4 | c.541+20T= (n.541+20T=)
| |
6 | g.79921605A>G | CA1640824948 | ELOVL4 | c.541+20T>C (n.541+20T>C)
| dbSNP |
6 | g.79921608T>C | CA3901518 | ELOVL4 | c.541+17A>G (n.541+17A>G)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921608T= | CA1640824950 | ELOVL4 | c.541+17A= (n.541+17A=)
| |
6 | g.79921609T>A | CA3901519 | ELOVL4 | c.541+16A>T (n.541+16A>T)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.79921609T= | CA1640824951 | ELOVL4 | c.541+16A= (n.541+16A=)
| |
6 | g.79921610C>A | CA568392514 | ELOVL4 | c.541+15G>T (n.541+15G>T)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.79921610C= | CA1640824952 | ELOVL4 | c.541+15G= (n.541+15G=)
| |
6 | g.79921611C>T | CA2573141258 | ELOVL4 | c.541+14G>A (n.541+14G>A)
| ClinVar dbSNP |
6 | g.79921612T>C | CA3901520 | ELOVL4 | c.541+13A>G (n.541+13A>G)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.79921612T= | CA1640824953 | ELOVL4 | c.541+13A= (n.541+13A=)
| |
6 | g.79921613G>C | CA2679489842 | ELOVL4 | c.541+12C>G (n.541+12C>G)
| gnomAD v4 |
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)
| |