| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319273 |
| Start |
97732725:97732725(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.113A>C |
| AA Mutation |
p.Asp38Ala(p.D38A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000319273 |
| Start |
97732723:97732723(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.111C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000319273 |
| Start |
97733734:97733734(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.135G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |