Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.51765768T>A | CA384887436 | SCN8A | c.2642T>A (p.Val881Glu) c.489T>A c.646T>A n.2770T>A c.2675T>A (p.Val892Glu) | |
12 | g.51765768T>C | CA318258 | SCN8A | c.2642T>C (p.Val881Ala) c.489T>C c.646T>C n.2770T>C c.2675T>C (p.Val892Ala) | dbSNP |
12 | g.51765768T>G | CA384887439 | SCN8A | c.2642T>G (p.Val881Gly) c.489T>G c.646T>G n.2770T>G c.2675T>G (p.Val892Gly) | |
12 | g.51765768T= | CA2036184091 | SCN8A | c.2642T= (p.Val881=) c.489T= c.646T= n.2770T= c.2675T= (p.Val892=) | |
12 | g.51765769G>A | CA480061307 | SCN8A | c.2643G>A (p.Val881=) c.490G>A c.647G>A n.2771G>A c.2676G>A (p.Val892=) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.51765769G>C | CA480061309 | SCN8A | c.2643G>C (p.Val881=) c.490G>C c.647G>C n.2771G>C c.2676G>C (p.Val892=) | |
12 | g.51765769G= | CA2036184092 | SCN8A | c.2643G= (p.Val881=) c.490G= c.647G= n.2771G= c.2676G= (p.Val892=) | |
12 | g.51765769G>T | CA480061310 | SCN8A | c.2643G>T (p.Val881=) c.490G>T c.647G>T n.2771G>T c.2676G>T (p.Val892=) | |
12 | g.51765770C>A | CA384887443 | SCN8A | c.2644C>A (p.Leu882Met) c.491C>A c.648C>A n.2772C>A c.2677C>A (p.Leu893Met) | |
12 | g.51765770C>G | CA384887446 | SCN8A | c.2644C>G (p.Leu882Val) c.491C>G c.648C>G n.2772C>G c.2677C>G (p.Leu893Val) | |
12 | g.51765770C>T | CA480061312 | SCN8A | c.2644C>T (p.Leu882=) c.491C>T c.648C>T n.2772C>T c.2677C>T (p.Leu893=) | |
12 | g.51765771T>A | CA384887451 | SCN8A | c.2645T>A (p.Leu882Gln) c.492T>A c.649T>A n.2773T>A c.2678T>A (p.Leu893Gln) | |
12 | g.51765771T>C | CA384887461 | SCN8A | c.2645T>C (p.Leu882Pro) c.492T>C c.649T>C n.2773T>C c.2678T>C (p.Leu893Pro) | |
12 | g.51765771T>G | CA384887464 | SCN8A | c.2645T>G (p.Leu882Arg) c.492T>G c.649T>G n.2773T>G c.2678T>G (p.Leu893Arg) | |
12 | g.51765772G>A | CA480061314 | SCN8A | c.2646G>A (p.Leu882=) c.493G>A c.650G>A n.2774G>A c.2679G>A (p.Leu893=) | |
12 | g.51765772G>C | CA480061315 | SCN8A | c.2646G>C (p.Leu882=) c.493G>C c.650G>C n.2774G>C c.2679G>C (p.Leu893=) | |
12 | g.51765772G>T | CA480061317 | SCN8A | c.2646G>T (p.Leu882=) c.493G>T c.650G>T n.2774G>T c.2679G>T (p.Leu893=) | COSMIC COSMIC |
12 | g.51765773G>A | CA384887477 | SCN8A | c.2647G>A (p.Ala883Thr) c.494G>A c.651G>A n.2775G>A c.2680G>A (p.Ala894Thr) | |
12 | g.51765773G>C | CA384887481 | SCN8A | c.2647G>C (p.Ala883Pro) c.494G>C c.651G>C n.2775G>C c.2680G>C (p.Ala894Pro) | |
12 | g.51765773G>T | CA384887470 | SCN8A | c.2647G>T (p.Ala883Ser) c.494G>T c.651G>T n.2775G>T c.2680G>T (p.Ala894Ser) | |
12 | g.51765774C>A | CA384887482 | SCN8A | c.2648C>A (p.Ala883Asp) c.495C>A c.652C>A n.2776C>A c.2681C>A (p.Ala894Asp) | |
12 | g.51765774C>G | CA384887484 | SCN8A | c.2648C>G (p.Ala883Gly) c.495C>G c.652C>G n.2776C>G c.2681C>G (p.Ala894Gly) | |
12 | g.51765774C>T | CA384887483 | SCN8A | c.2648C>T (p.Ala883Val) c.495C>T c.652C>T n.2776C>T c.2681C>T (p.Ala894Val) | |
12 | g.51765775C>A | CA480061318 | SCN8A | c.2649C>A (p.Ala883=) c.496C>A c.653C>A n.2777C>A c.2682C>A (p.Ala894=) | |
12 | g.51765775C>G | CA480061320 | SCN8A | c.2649C>G (p.Ala883=) c.496C>G c.653C>G n.2777C>G c.2682C>G (p.Ala894=) | |
12 | g.51765775C>T | CA480061322 | SCN8A | c.2649C>T (p.Ala883=) c.496C>T c.653C>T n.2777C>T c.2682C>T (p.Ala894=) | |
12 | g.51765776A>C | CA384887487 | SCN8A | c.2650A>C (p.Ile884Leu) c.497A>C c.654A>C n.2778A>C c.2683A>C (p.Ile895Leu) | |
12 | g.51765776A>G | CA384887488 | SCN8A | c.2650A>G (p.Ile884Val) c.497A>G c.654A>G n.2778A>G c.2683A>G (p.Ile895Val) | |
12 | g.51765776A>T | CA384887489 | SCN8A | c.2650A>T (p.Ile884Phe) c.497A>T c.654A>T n.2778A>T c.2683A>T (p.Ile895Phe) | |
12 | g.51765777T>A | CA384887490 | SCN8A | c.2651T>A (p.Ile884Asn) c.498T>A c.655T>A n.2779T>A c.2684T>A (p.Ile895Asn) | |
12 | g.51765777T>C | CA384887491 | SCN8A | c.2651T>C (p.Ile884Thr) c.498T>C c.655T>C n.2779T>C c.2684T>C (p.Ile895Thr) | |
12 | g.51765777T>G | CA384887494 | SCN8A | c.2651T>G (p.Ile884Ser) c.498T>G c.655T>G n.2779T>G c.2684T>G (p.Ile895Ser) | |
12 | g.51765778T>A | CA480061327 | SCN8A | c.2652T>A (p.Ile884=) c.499T>A c.656T>A n.2780T>A c.2685T>A (p.Ile895=) | |
12 | g.51765778T>C | CA480061329 | SCN8A | c.2652T>C (p.Ile884=) c.499T>C c.656T>C n.2780T>C c.2685T>C (p.Ile895=) | |
12 | g.51765778T>G | CA384887498 | SCN8A | c.2652T>G (p.Ile884Met) c.499T>G c.656T>G n.2780T>G c.2685T>G (p.Ile895Met) | |
12 | g.51765779A>C | CA384887500 | SCN8A | c.2653A>C (p.Ile885Leu) c.500A>C c.657A>C n.2781A>C c.2686A>C (p.Ile896Leu) | |
12 | g.51765779A>G | CA384887502 | SCN8A | c.2653A>G (p.Ile885Val) c.500A>G c.657A>G n.2781A>G c.2686A>G (p.Ile896Val) | gnomAD v4 |
12 | g.51765779A>T | CA384887505 | SCN8A | c.2653A>T (p.Ile885Phe) c.500A>T c.657A>T n.2781A>T c.2686A>T (p.Ile896Phe) | |
12 | g.51765780T>A | CA384887507 | SCN8A | c.2654T>A (p.Ile885Asn) c.501T>A c.658T>A n.2782T>A c.2687T>A (p.Ile896Asn) | |
12 | g.51765780T>C | CA384887511 | SCN8A | c.2654T>C (p.Ile885Thr) c.501T>C c.658T>C n.2782T>C c.2687T>C (p.Ile896Thr) | ClinVar dbSNP |
12 | g.51765780T>G | CA384887514 | SCN8A | c.2654T>G (p.Ile885Ser) c.501T>G c.658T>G n.2782T>G c.2687T>G (p.Ile896Ser) | |
12 | g.51765780T= | CA2036184098 | SCN8A | c.2654T= (p.Ile885=) c.501T= c.658T= n.2782T= c.2687T= (p.Ile896=) | |
12 | g.51765781T>A | CA480061331 | SCN8A | c.2655T>A (p.Ile885=) c.502T>A c.659T>A n.2783T>A c.2688T>A (p.Ile896=) | |
12 | g.51765781T>C | CA480061332 | SCN8A | c.2655T>C (p.Ile885=) c.502T>C c.659T>C n.2783T>C c.2688T>C (p.Ile896=) | |
12 | g.51765781T>G | CA384887517 | SCN8A | c.2655T>G (p.Ile885Met) c.502T>G c.659T>G n.2783T>G c.2688T>G (p.Ile896Met) | |
12 | g.51765782G>A | CA384887521 | SCN8A | c.2656G>A (p.Val886Ile) c.503G>A c.660G>A n.2784G>A c.2689G>A (p.Val897Ile) | |
12 | g.51765782G>C | CA384887525 | SCN8A | c.2656G>C (p.Val886Leu) c.503G>C c.660G>C n.2784G>C c.2689G>C (p.Val897Leu) | |
12 | g.51765782G>T | CA384887527 | SCN8A | c.2656G>T (p.Val886Phe) c.503G>T c.660G>T n.2784G>T c.2689G>T (p.Val897Phe) | |
12 | g.51765783T>A | CA384887528 | SCN8A | c.2657T>A (p.Val886Asp) c.504T>A c.661T>A n.2785T>A c.2690T>A (p.Val897Asp) | |
12 | g.51765783T>C | CA384887529 | SCN8A | c.2657T>C (p.Val886Ala) c.504T>C c.661T>C n.2785T>C c.2690T>C (p.Val897Ala) |