Gene >> FHIT
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000468189 |
| Start |
60014134:60014134(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.122T>C |
| AA Mutation |
p.Leu41Pro(p.L41P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000468189 |
| Start |
60011402:60011402(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.250-2A>G |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |