Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.87811447_87811455del | CA2578140102 | IBSP | c.491_499del (p.Glu164_Glu166del) | |
4 | g.87811450G>A | CA357620659 | IBSP | c.494G>A (p.Ser165Asn) | gnomAD v4 |
4 | g.87811450G>C | CA357620660 | IBSP | c.494G>C (p.Ser165Thr) | |
4 | g.87811450G>T | CA357620662 | IBSP | c.494G>T (p.Ser165Ile) | |
4 | g.87811451C>A | CA3002401 | IBSP | c.495C>A (p.Ser165Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.87811451C= | CA1474474591 | IBSP | c.495C= (p.Ser165=) | |
4 | g.87811451C>G | CA357620665 | IBSP | c.495C>G (p.Ser165Arg) | |
4 | g.87811451C>T | CA100855675 | IBSP | c.495C>T (p.Ser165=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.87811452G>A | CA100855693 | IBSP | c.496G>A (p.Glu166Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.87811452G>C | CA357620667 | IBSP | c.496G>C (p.Glu166Gln) | |
4 | g.87811452G= | CA1474474592 | IBSP | c.496G= (p.Glu166=) | |
4 | g.87811452G>T | CA357620669 | IBSP | c.496G>T (p.Glu166Ter) | dbSNP |
4 | g.87811453A>C | CA357620671 | IBSP | c.497A>C (p.Glu166Ala) | |
4 | g.87811453A>G | CA357620672 | IBSP | c.497A>G (p.Glu166Gly) | |
4 | g.87811453A>T | CA357620674 | IBSP | c.497A>T (p.Glu166Val) | |
4 | g.87811453_87811456delinsAAGC | CA1474474593 | IBSP | c.497_500delinsAAGC (p.Glu166=) | |
4 | g.87811454A>C | CA357620676 | IBSP | c.498A>C (p.Glu166Asp) | |
4 | g.87811454A>G | CA440295701 | IBSP | c.498A>G (p.Glu166=) | |
4 | g.87811454A>T | CA357620677 | IBSP | c.498A>T (p.Glu166Asp) | |
4 | g.87811456_87811458del | CA1065112451 | IBSP | c.500_502del (p.Ala167del) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.87811455G>A | CA357620682 | IBSP | c.499G>A (p.Ala167Thr) | COSMIC |
4 | g.87811455G>C | CA357620681 | IBSP | c.499G>C (p.Ala167Pro) | |
4 | g.87811455G>T | CA357620679 | IBSP | c.499G>T (p.Ala167Ser) | |
4 | g.87811456C>A | CA3002402 | IBSP | c.500C>A (p.Ala167Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.87811456C= | CA1474474594 | IBSP | c.500C= (p.Ala167=) | |
4 | g.87811456C>G | CA357620683 | IBSP | c.500C>G (p.Ala167Gly) | |
4 | g.87811456C>T | CA357620686 | IBSP | c.500C>T (p.Ala167Val) | |
4 | g.87811457A= | CA1474474595 | IBSP | c.501A= (p.Ala167=) | |
4 | g.87811457A>C | CA3002403 | IBSP | c.501A>C (p.Ala167=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.87811457A>G | CA440295703 | IBSP | c.501A>G (p.Ala167=) | gnomAD v4 |
4 | g.87811457A>T | CA440295704 | IBSP | c.501A>T (p.Ala167=) | |
4 | g.87811458G>A | CA357620688 | IBSP | c.502G>A (p.Glu168Lys) | |
4 | g.87811458G>C | CA357620690 | IBSP | c.502G>C (p.Glu168Gln) | |
4 | g.87811458G>T | CA357620691 | IBSP | c.502G>T (p.Glu168Ter) | |
4 | g.87811459A>C | CA357620692 | IBSP | c.503A>C (p.Glu168Ala) | |
4 | g.87811459A>G | CA357620693 | IBSP | c.503A>G (p.Glu168Gly) | |
4 | g.87811459A>T | CA357620695 | IBSP | c.503A>T (p.Glu168Val) | |
4 | g.87811460A>C | CA357620696 | IBSP | c.504A>C (p.Glu168Asp) | |
4 | g.87811460A>G | CA440295711 | IBSP | c.504A>G (p.Glu168=) | |
4 | g.87811460A>T | CA357620698 | IBSP | c.504A>T (p.Glu168Asp) | |
4 | g.87811461G>A | CA357620699 | IBSP | c.505G>A (p.Val169Met) | |
4 | g.87811461G>C | CA357620701 | IBSP | c.505G>C (p.Val169Leu) | |
4 | g.87811461G= | CA1474474596 | IBSP | c.505G= (p.Val169=) | |
4 | g.87811461G>T | CA357620702 | IBSP | c.505G>T (p.Val169Leu) | dbSNP gnomAD v4 |
4 | g.87811462T>A | CA357620705 | IBSP | c.506T>A (p.Val169Glu) | |
4 | g.87811462T>C | CA357620706 | IBSP | c.506T>C (p.Val169Ala) | |
4 | g.87811462T>G | CA3002404 | IBSP | c.506T>G (p.Val169Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.87811462T= | CA1474474597 | IBSP | c.506T= (p.Val169=) | |
4 | g.87811463G>A | CA440295716 | IBSP | c.507G>A (p.Val169=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
4 | g.87811463G>C | CA440295717 | IBSP | c.507G>C (p.Val169=) |