Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23423672G>A | CA485766590 | MYH7 | c.2974C>T (p.Leu992=) n.3080C>T | |
14 | g.23423672G>C | CA389046367 | MYH7 | c.2974C>G (p.Leu992Val) n.3080C>G | |
14 | g.23423672G= | CA2123453366 | MYH7 | c.2974C= (p.Leu992=) n.3080C= | |
14 | g.23423672G>T | CA013260 | MYH7 | c.2974C>A (p.Leu992Met) n.3080C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23423673C>A | CA013250 | MYH7 | c.2973G>T (p.Lys991Asn) n.3079G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.23423673C= | CA2123453376 | MYH7 | c.2973G= (p.Lys991=) n.3079G= | |
14 | g.23423673C>G | CA389046370 | MYH7 | c.2973G>C (p.Lys991Asn) n.3079G>C | |
14 | g.23423673C>T | CA485766591 | MYH7 | c.2973G>A (p.Lys991=) n.3079G>A | COSMIC |
14 | g.23423674T>A | CA389046371 | MYH7 | c.2972A>T (p.Lys991Met) n.3078A>T | |
14 | g.23423674T>C | CA035021 | MYH7 | c.2972A>G (p.Lys991Arg) n.3078A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23423674T>G | CA389046372 | MYH7 | c.2972A>C (p.Lys991Thr) n.3078A>C | |
14 | g.23423674T= | CA2123453379 | MYH7 | c.2972A= (p.Lys991=) n.3078A= | |
14 | g.23423675T>A | CA389046375 | MYH7 | c.2971A>T (p.Lys991Ter) n.3077A>T | |
14 | g.23423675T>C | CA389046377 | MYH7 | c.2971A>G (p.Lys991Glu) n.3077A>G | |
14 | g.23423675T>G | CA389046374 | MYH7 | c.2971A>C (p.Lys991Gln) n.3077A>C | gnomAD v4 |
14 | g.23423676G>A | CA485766592 | MYH7 | c.2970C>T (p.Ala990=) n.3076C>T | gnomAD v4 |
14 | g.23423676G>C | CA485766593 | MYH7 | c.2970C>G (p.Ala990=) n.3076C>G | |
14 | g.23423676G>T | CA485766594 | MYH7 | c.2970C>A (p.Ala990=) n.3076C>A | |
14 | g.23423677G>A | CA389046378 | MYH7 | c.2969C>T (p.Ala990Val) n.3075C>T | dbSNP |
14 | g.23423677G>C | CA389046379 | MYH7 | c.2969C>G (p.Ala990Gly) n.3075C>G | |
14 | g.23423677G= | CA2123453381 | MYH7 | c.2969C= (p.Ala990=) n.3075C= | |
14 | g.23423677G>T | CA389046380 | MYH7 | c.2969C>A (p.Ala990Asp) n.3075C>A | |
14 | g.23423678C>A | CA389046382 | MYH7 | c.2968G>T (p.Ala990Ser) n.3074G>T | gnomAD v4 |
14 | g.23423678C= | CA2123453385 | MYH7 | c.2968G= (p.Ala990=) n.3074G= | |
14 | g.23423678C>G | CA389046384 | MYH7 | c.2968G>C (p.Ala990Pro) n.3074G>C | |
14 | g.23423678C>T | CA035008 | MYH7 | c.2968G>A (p.Ala990Thr) n.3074G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23423678_23423679delinsGG | CA2697553843 | MYH7 | c.2967_2968delinsCC (p.Ala990Pro) n.3073_3074delinsCC | ClinVar |
14 | g.23423678_23423679delinsTG | CA915946996 | MYH7 | c.2967_2968delinsCA (p.Ala990Thr) n.3073_3074delinsCA | ClinVar |
14 | g.23423679A= | CA2123453391 | MYH7 | c.2967T= (p.Ile989=) n.3073T= | |
14 | g.23423679A>C | CA389046386 | MYH7 | c.2967T>G (p.Ile989Met) n.3073T>G | |
14 | g.23423679A>G | CA013242 | MYH7 | c.2967T>C (p.Ile989=) n.3073T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23423679A>T | CA485766595 | MYH7 | c.2967T>A (p.Ile989=) n.3073T>A | |
14 | g.23423680A>C | CA389046387 | MYH7 | c.2966T>G (p.Ile989Ser) n.3072T>G | |
14 | g.23423680A>G | CA389046389 | MYH7 | c.2966T>C (p.Ile989Thr) n.3072T>C | |
14 | g.23423680A>T | CA389046390 | MYH7 | c.2966T>A (p.Ile989Asn) n.3072T>A | |
14 | g.23423681T>A | CA389046391 | MYH7 | c.2965A>T (p.Ile989Phe) n.3071A>T | |
14 | g.23423681T>C | CA389046392 | MYH7 | c.2965A>G (p.Ile989Val) n.3071A>G | |
14 | g.23423681T>G | CA389046394 | MYH7 | c.2965A>C (p.Ile989Leu) n.3071A>C | |
14 | g.23423682G>A | CA257818753 | MYH7 | c.2964C>T (p.Ile988=) n.3070C>T | dbSNP |
14 | g.23423682G>C | CA389046396 | MYH7 | c.2964C>G (p.Ile988Met) n.3070C>G | |
14 | g.23423682G= | CA2123453396 | MYH7 | c.2964C= (p.Ile988=) n.3070C= | |
14 | g.23423682G>T | CA485766596 | MYH7 | c.2964C>A (p.Ile988=) n.3070C>A | |
14 | g.23423683A= | CA2123453401 | MYH7 | c.2963T= (p.Ile988=) n.3069T= | |
14 | g.23423683A>C | CA16619848 | MYH7 | c.2963T>G (p.Ile988Ser) n.3069T>G | ClinVar dbSNP |
14 | g.23423683A>G | CA389046400 | MYH7 | c.2963T>C (p.Ile988Thr) n.3069T>C | |
14 | g.23423683A>T | CA389046398 | MYH7 | c.2963T>A (p.Ile988Asn) n.3069T>A | |
14 | g.23423684T>A | CA389046402 | MYH7 | c.2962A>T (p.Ile988Phe) n.3068A>T | |
14 | g.23423684T>C | CA389046404 | MYH7 | c.2962A>G (p.Ile988Val) n.3068A>G | gnomAD v4 |
14 | g.23423684T>G | CA389046405 | MYH7 | c.2962A>C (p.Ile988Leu) n.3068A>C | |
14 | g.23423685C>A | CA389046407 | MYH7 | c.2961G>T (p.Glu987Asp) n.3067G>T |