Gene >> CTHRC1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330295 |
| Start |
103382497:103382497(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.629A>T |
| AA Mutation |
p.Asp210Val(p.D210V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330295 |
| Start |
103371787:103371787(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.131A>G |
| AA Mutation |
p.Gln44Arg(p.Q44R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |