| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357115 |
| Start |
151014539:151014539(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.104T>C |
| AA Mutation |
p.Leu35Pro(p.L35P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357115 |
| Start |
150848892:150848892(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.4265C>T |
| AA Mutation |
p.Ser1422Phe(p.S1422F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357115 |
| Start |
150277861:150277861(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs76608264
|
| CDS Mutation |
c.8493C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |