| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260061 |
| Start |
76660897:76660897(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.696C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260061 |
| Start |
76665925:76665925(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs533407564
|
| CDS Mutation |
c.30C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260061 |
| Start |
76661122:76661122(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.471G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |