Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.2326105C>A | CA394352205 | ABCA3 | c.224G>T (p.Gly75Val) n.787G>T | |
16 | g.2326105C>G | CA394352208 | ABCA3 | c.224G>C (p.Gly75Ala) n.787G>C | |
16 | g.2326105C>T | CA394352209 | ABCA3 | c.224G>A (p.Gly75Glu) n.787G>A | |
16 | g.2326106C>A | CA394352213 | ABCA3 | c.223G>T (p.Gly75Ter) n.786G>T | |
16 | g.2326106C>G | CA394352215 | ABCA3 | c.223G>C (p.Gly75Arg) n.786G>C | |
16 | g.2326106C>T | CA394352212 | ABCA3 | c.223G>A (p.Gly75Arg) n.786G>A | |
16 | g.2326107T>A | CA493361758 | ABCA3 | c.222A>T (p.Pro74=) n.785A>T | |
16 | g.2326107T>C | CA493361762 | ABCA3 | c.222A>G (p.Pro74=) n.785A>G | |
16 | g.2326107T>G | CA493361760 | ABCA3 | c.222A>C (p.Pro74=) n.785A>C | |
16 | g.2326108G>A | CA394352217 | ABCA3 | c.221C>T (p.Pro74Leu) n.784C>T | |
16 | g.2326108G>C | CA394352223 | ABCA3 | c.221C>G (p.Pro74Arg) n.784C>G | |
16 | g.2326108G>T | CA394352220 | ABCA3 | c.221C>A (p.Pro74Gln) n.784C>A | |
16 | g.2326109G>A | CA394352225 | ABCA3 | c.220C>T (p.Pro74Ser) n.783C>T | dbSNP gnomAD v2 gnomAD v4 |
16 | g.2326109G>C | CA394352229 | ABCA3 | c.220C>G (p.Pro74Ala) n.783C>G | |
16 | g.2326109G= | CA2202173466 | ABCA3 | c.220C= (p.Pro74=) n.783C= | |
16 | g.2326109G>T | CA394352227 | ABCA3 | c.220C>A (p.Pro74Thr) n.783C>A | COSMIC |
16 | g.2326110C>A | CA276853752 | ABCA3 | c.219G>T (p.Pro73=) n.782G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.2326110C= | CA2202173471 | ABCA3 | c.219G= (p.Pro73=) n.782G= | |
16 | g.2326110C>G | CA493361770 | ABCA3 | c.219G>C (p.Pro73=) n.782G>C | |
16 | g.2326110C>T | CA7841759 | ABCA3 | c.219G>A (p.Pro73=) n.782G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.2326110dup | CA719179515 | ABCA3 | c.219dup (p.Pro74AlafsTer15) n.782dup | dbSNP |
16 | g.2326111G>A | CA7841760 | ABCA3 | c.218C>T (p.Pro73Leu) n.781C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.2326111G>C | CA394352236 | ABCA3 | c.218C>G (p.Pro73Arg) n.781C>G | |
16 | g.2326111G= | CA2202173478 | ABCA3 | c.218C= (p.Pro73=) n.781C= | |
16 | g.2326111G>T | CA394352238 | ABCA3 | c.218C>A (p.Pro73Gln) n.781C>A | |
16 | g.2326112G>A | CA7841761 | ABCA3 | c.217C>T (p.Pro73Ser) n.780C>T | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
16 | g.2326112G>C | CA394352242 | ABCA3 | c.217C>G (p.Pro73Ala) n.780C>G | |
16 | g.2326112G= | CA2202173483 | ABCA3 | c.217C= (p.Pro73=) n.780C= | |
16 | g.2326112G>T | CA7841762 | ABCA3 | c.217C>A (p.Pro73Thr) n.780C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.2326113A= | CA2202173488 | ABCA3 | c.216T= (p.Pro72=) n.779T= | |
16 | g.2326113A>C | CA493361779 | ABCA3 | c.216T>G (p.Pro72=) n.779T>G | |
16 | g.2326113A>G | CA493361781 | ABCA3 | c.216T>C (p.Pro72=) n.779T>C | |
16 | g.2326113A>T | CA493361782 | ABCA3 | c.216T>A (p.Pro72=) n.779T>A | |
16 | g.2326114G>A | CA276853777 | ABCA3 | c.215C>T (p.Pro72Leu) n.778C>T | dbSNP gnomAD v3 gnomAD v4 COSMIC |
16 | g.2326114G>C | CA394352248 | ABCA3 | c.215C>G (p.Pro72Arg) n.778C>G | gnomAD v4 COSMIC |
16 | g.2326114G= | CA2202173493 | ABCA3 | c.215C= (p.Pro72=) n.778C= | |
16 | g.2326114G>T | CA394352249 | ABCA3 | c.215C>A (p.Pro72His) n.778C>A | |
16 | g.2326116dup | CA2202173494 | ABCA3 | c.215dup (p.Pro73SerfsTer16) n.778dup | dbSNP |
16 | g.2326115G>A | CA394352250 | ABCA3 | c.214C>T (p.Pro72Ser) n.777C>T | dbSNP gnomAD v3 gnomAD v4 |
16 | g.2326115G>C | CA394352255 | ABCA3 | c.214C>G (p.Pro72Ala) n.777C>G | |
16 | g.2326115G= | CA2202173499 | ABCA3 | c.214C= (p.Pro72=) n.777C= | |
16 | g.2326115G>T | CA394352252 | ABCA3 | c.214C>A (p.Pro72Thr) n.777C>A | gnomAD v4 |
16 | g.2326116G>A | CA7841763 | ABCA3 | c.213C>T (p.Phe71=) n.776C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.2326116G>C | CA394352257 | ABCA3 | c.213C>G (p.Phe71Leu) n.776C>G | |
16 | g.2326116G= | CA2202173503 | ABCA3 | c.213C= (p.Phe71=) n.776C= | |
16 | g.2326116G>T | CA394352260 | ABCA3 | c.213C>A (p.Phe71Leu) n.776C>A | |
16 | g.2326117A>C | CA394352262 | ABCA3 | c.212T>G (p.Phe71Cys) n.775T>G | |
16 | g.2326117A>G | CA394352264 | ABCA3 | c.212T>C (p.Phe71Ser) n.775T>C | |
16 | g.2326117A>T | CA394352266 | ABCA3 | c.212T>A (p.Phe71Tyr) n.775T>A | |
16 | g.2326118A>C | CA394352268 | ABCA3 | c.211T>G (p.Phe71Val) n.774T>G |