| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330295 |
| Start |
103375805:103375805(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.218G>A |
| AA Mutation |
p.Gly73Asp(p.G73D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000330295 |
| Start |
103375890:103375890(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.303C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000330295 |
| Start |
103378095:103378095(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769625099
|
| CDS Mutation |
c.441A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |