| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 |