| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341935 |
| Start |
167136343:167136343(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.113T>C |
| AA Mutation |
p.Leu38Ser(p.L38S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341935 |
| Start |
167136795:167136795(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.565T>C |
| AA Mutation |
p.Tyr189His(p.Y189H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000341935 |
| Start |
167136950:167136950(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.720C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |