Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768103G>A | CA389475947 | FOXG1 | c.824G>A (p.Arg275His) | dbSNP |
14 | g.28768103G>C | CA389475948 | FOXG1 | c.824G>C (p.Arg275Pro) | ClinVar dbSNP |
14 | g.28768103G= | CA2126000282 | FOXG1 | c.824G= (p.Arg275=) | |
14 | g.28768103G>T | CA389475949 | FOXG1 | c.824G>T (p.Arg275Leu) | |
14 | g.28768104C>A | CA486099016 | FOXG1 | c.825C>A (p.Arg275=) | |
14 | g.28768104C>G | CA486099015 | FOXG1 | c.825C>G (p.Arg275=) | |
14 | g.28768104C>T | CA486099014 | FOXG1 | c.825C>T (p.Arg275=) | gnomAD v4 COSMIC |
14 | g.28768105C>A | CA389475951 | FOXG1 | c.826C>A (p.Arg276Ser) | |
14 | g.28768105C>G | CA389475952 | FOXG1 | c.826C>G (p.Arg276Gly) | |
14 | g.28768105C>T | CA389475950 | FOXG1 | c.826C>T (p.Arg276Cys) | ClinVar dbSNP |
14 | g.28768106G>A | CA389475955 | FOXG1 | c.827G>A (p.Arg276His) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768106G>C | CA389475953 | FOXG1 | c.827G>C (p.Arg276Pro) | |
14 | g.28768106G= | CA2126000283 | FOXG1 | c.827G= (p.Arg276=) | |
14 | g.28768106G>T | CA389475954 | FOXG1 | c.827G>T (p.Arg276Leu) | gnomAD v4 |
14 | g.28768107C>A | CA486099025 | FOXG1 | c.828C>A (p.Arg276=) | |
14 | g.28768107C= | CA2126000284 | FOXG1 | c.828C= (p.Arg276=) | |
14 | g.28768107C>G | CA486099024 | FOXG1 | c.828C>G (p.Arg276=) | |
14 | g.28768107C>T | CA486099022 | FOXG1 | c.828C>T (p.Arg276=) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768108T>A | CA389475956 | FOXG1 | c.829T>A (p.Ser277Thr) | |
14 | g.28768108T>C | CA389475957 | FOXG1 | c.829T>C (p.Ser277Pro) | |
14 | g.28768108T>G | CA389475958 | FOXG1 | c.829T>G (p.Ser277Ala) | |
14 | g.28768109C>A | CA389475959 | FOXG1 | c.830C>A (p.Ser277Tyr) | |
14 | g.28768109C>G | CA389475960 | FOXG1 | c.830C>G (p.Ser277Cys) | |
14 | g.28768109C>T | CA389475961 | FOXG1 | c.830C>T (p.Ser277Phe) | |
14 | g.28768110C>A | CA486099033 | FOXG1 | c.831C>A (p.Ser277=) | |
14 | g.28768110C>G | CA486099035 | FOXG1 | c.831C>G (p.Ser277=) | |
14 | g.28768110C>T | CA486099034 | FOXG1 | c.831C>T (p.Ser277=) | |
14 | g.28768111A>C | CA389475962 | FOXG1 | c.832A>C (p.Thr278Pro) | |
14 | g.28768111A>G | CA389475963 | FOXG1 | c.832A>G (p.Thr278Ala) | COSMIC |
14 | g.28768111A>T | CA389475964 | FOXG1 | c.832A>T (p.Thr278Ser) | |
14 | g.28768112C>A | CA389475965 | FOXG1 | c.833C>A (p.Thr278Asn) | |
14 | g.28768112C>G | CA389475966 | FOXG1 | c.833C>G (p.Thr278Ser) | |
14 | g.28768112C>T | CA389475967 | FOXG1 | c.833C>T (p.Thr278Ile) | gnomAD v4 |
14 | g.28768113C>A | CA486099042 | FOXG1 | c.834C>A (p.Thr278=) | |
14 | g.28768113C= | CA2126000285 | FOXG1 | c.834C= (p.Thr278=) | |
14 | g.28768113C>G | CA486099043 | FOXG1 | c.834C>G (p.Thr278=) | |
14 | g.28768113C>T | CA7140632 | FOXG1 | c.834C>T (p.Thr278=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768114A>C | CA389475968 | FOXG1 | c.835A>C (p.Thr279Pro) | |
14 | g.28768114A>G | CA389475969 | FOXG1 | c.835A>G (p.Thr279Ala) | |
14 | g.28768114A>T | CA389475970 | FOXG1 | c.835A>T (p.Thr279Ser) | |
14 | g.28768115C>A | CA389475971 | FOXG1 | c.836C>A (p.Thr279Asn) | ClinVar gnomAD v4 COSMIC |
14 | g.28768115C>G | CA389475972 | FOXG1 | c.836C>G (p.Thr279Ser) | |
14 | g.28768115C>T | CA389475973 | FOXG1 | c.836C>T (p.Thr279Ile) | |
14 | g.28768116C>A | CA486099049 | FOXG1 | c.837C>A (p.Thr279=) | |
14 | g.28768116C= | CA2126000286 | FOXG1 | c.837C= (p.Thr279=) | |
14 | g.28768116C>G | CA486099051 | FOXG1 | c.837C>G (p.Thr279=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768116C>T | CA7140633 | FOXG1 | c.837C>T (p.Thr279=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.28768117T>A | CA389475974 | FOXG1 | c.838T>A (p.Ser280Thr) | |
14 | g.28768117T>C | CA389475975 | FOXG1 | c.838T>C (p.Ser280Pro) | |
14 | g.28768117T>G | CA389475976 | FOXG1 | c.838T>G (p.Ser280Ala) |