| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000280187 |
| Start |
175635026:175635026(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.716G>T |
| AA Mutation |
p.Trp239Leu(p.W239L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280187 |
| Start |
175635010:175635010(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs141777363
|
| CDS Mutation |
c.732C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000280187 |
| Start |
175635022:175635022(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.720C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |