Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23417576T>A | CA014757 | MHRT,MYH7 | c.4280A>T (p.Asp1427Val) n.857T>A | dbSNP |
14 | g.23417576T>C | CA389040247 | MHRT,MYH7 | c.4280A>G (p.Asp1427Gly) n.857T>C | |
14 | g.23417576T>G | CA389040245 | MHRT,MYH7 | c.4280A>C (p.Asp1427Ala) n.857T>G | |
14 | g.23417576T= | CA2123469571 | MHRT,MYH7 | c.4280A= (p.Asp1427=) n.857T= | |
14 | g.23417577C>A | CA389040248 | MHRT,MYH7 | c.4279G>T (p.Asp1427Tyr) n.858C>A | ClinVar |
14 | g.23417577C>G | CA389040249 | MHRT,MYH7 | c.4279G>C (p.Asp1427His) n.858C>G | |
14 | g.23417577C>T | CA389040251 | MHRT,MYH7 | c.4279G>A (p.Asp1427Asn) n.858C>T | ClinVar |
14 | g.23417578C>A | CA389040252 | MHRT,MYH7 | c.4278G>T (p.Glu1426Asp) n.859C>A | |
14 | g.23417578C= | CA2123469577 | MHRT,MYH7 | c.4278G= (p.Glu1426=) n.859C= | |
14 | g.23417578C>G | CA389040254 | MHRT,MYH7 | c.4278G>C (p.Glu1426Asp) n.859C>G | |
14 | g.23417578C>T | CA041463 | MHRT,MYH7 | c.4278G>A (p.Glu1426=) n.859C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23417579T>A | CA389040256 | MHRT,MYH7 | c.4277A>T (p.Glu1426Val) n.860T>A | |
14 | g.23417579T>C | CA389040257 | MHRT,MYH7 | c.4277A>G (p.Glu1426Gly) n.860T>C | |
14 | g.23417579T>G | CA389040259 | MHRT,MYH7 | c.4277A>C (p.Glu1426Ala) n.860T>G | |
14 | g.23417580C>A | CA389040261 | MHRT,MYH7 | c.4276G>T (p.Glu1426Ter) n.861C>A | gnomAD v4 |
14 | g.23417580C= | CA2123469586 | MHRT,MYH7 | c.4276G= (p.Glu1426=) n.861C= | |
14 | g.23417580C>G | CA389040263 | MHRT,MYH7 | c.4276G>C (p.Glu1426Gln) n.861C>G | |
14 | g.23417580C>T | CA014743 | MHRT,MYH7 | c.4276G>A (p.Glu1426Lys) n.861C>T | ClinVar dbSNP COSMIC |
14 | g.23417581G>A | CA041447 | MHRT,MYH7 | c.4275C>T (p.Ile1425=) n.862G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23417581G>C | CA389040265 | MHRT,MYH7 | c.4275C>G (p.Ile1425Met) n.862G>C | |
14 | g.23417581G= | CA2123469597 | MHRT,MYH7 | c.4275C= (p.Ile1425=) n.862G= | |
14 | g.23417581G>T | CA041432 | MHRT,MYH7 | c.4275C>A (p.Ile1425=) n.862G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23417582A>C | CA389040266 | MHRT,MYH7 | c.4274T>G (p.Ile1425Ser) n.863A>C | |
14 | g.23417582A>G | CA389040268 | MHRT,MYH7 | c.4274T>C (p.Ile1425Thr) n.863A>G | |
14 | g.23417582A>T | CA389040269 | MHRT,MYH7 | c.4274T>A (p.Ile1425Asn) n.863A>T | |
14 | g.23417583T>A | CA389040271 | MHRT,MYH7 | c.4273A>T (p.Ile1425Phe) n.864T>A | gnomAD v4 |
14 | g.23417583T>C | CA389040272 | MHRT,MYH7 | c.4273A>G (p.Ile1425Val) n.864T>C | |
14 | g.23417583T>G | CA389040273 | MHRT,MYH7 | c.4273A>C (p.Ile1425Leu) n.864T>G | |
14 | g.23417584C>A | CA389040274 | MHRT,MYH7 | c.4272G>T (p.Glu1424Asp) n.865C>A | |
14 | g.23417584C>G | CA389040275 | MHRT,MYH7 | c.4272G>C (p.Glu1424Asp) n.865C>G | |
14 | g.23417584C>T | CA485617815 | MHRT,MYH7 | c.4272G>A (p.Glu1424=) n.865C>T | |
14 | g.23417585T>A | CA389040277 | MHRT,MYH7 | c.4271A>T (p.Glu1424Val) n.866T>A | ClinVar |
14 | g.23417585T>C | CA389040278 | MHRT,MYH7 | c.4271A>G (p.Glu1424Gly) n.866T>C | |
14 | g.23417585T>G | CA389040279 | MHRT,MYH7 | c.4271A>C (p.Glu1424Ala) n.866T>G | |
14 | g.23417586C>A | CA389040281 | MHRT,MYH7 | c.4270G>T (p.Glu1424Ter) n.867C>A | |
14 | g.23417586C= | CA2123469604 | MHRT,MYH7 | c.4270G= (p.Glu1424=) n.867C= | |
14 | g.23417586C>G | CA389040283 | MHRT,MYH7 | c.4270G>C (p.Glu1424Gln) n.867C>G | |
14 | g.23417586C>T | CA014734 | MHRT,MYH7 | c.4270G>A (p.Glu1424Lys) n.867C>T | ClinVar dbSNP COSMIC |
14 | g.23417587A= | CA2123469610 | MHRT,MYH7 | c.4269T= (p.Asn1423=) n.868A= | |
14 | g.23417587A>C | CA389040285 | MHRT,MYH7 | c.4269T>G (p.Asn1423Lys) n.868A>C | dbSNP gnomAD v4 |
14 | g.23417587A>G | CA485617819 | MHRT,MYH7 | c.4269T>C (p.Asn1423=) n.868A>G | dbSNP |
14 | g.23417587A>T | CA389040286 | MHRT,MYH7 | c.4269T>A (p.Asn1423Lys) n.868A>T | |
14 | g.23417588T>A | CA389040288 | MHRT,MYH7 | c.4268A>T (p.Asn1423Ile) n.869T>A | |
14 | g.23417588T>C | CA389040290 | MHRT,MYH7 | c.4268A>G (p.Asn1423Ser) n.869T>C | |
14 | g.23417588T>G | CA389040291 | MHRT,MYH7 | c.4268A>C (p.Asn1423Thr) n.869T>G | |
14 | g.23417589T>A | CA389040293 | MHRT,MYH7 | c.4267A>T (p.Asn1423Tyr) n.870T>A | |
14 | g.23417589T>C | CA389040294 | MHRT,MYH7 | c.4267A>G (p.Asn1423Asp) n.870T>C | |
14 | g.23417589T>G | CA389040296 | MHRT,MYH7 | c.4267A>C (p.Asn1423His) n.870T>G | |
14 | g.23417590C>A | CA389040297 | MHRT,MYH7 | c.4266G>T (p.Gln1422His) n.871C>A | |
14 | g.23417590C>G | CA389040299 | MHRT,MYH7 | c.4266G>C (p.Gln1422His) n.871C>G |