| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222800 |
| Start |
73737334:73737334(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142499119
|
| CDS Mutation |
c.520G>A |
| AA Mutation |
p.Val174Ile(p.V174I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000222800 |
| Start |
73738723:73738723(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.75C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000222800 |
| Start |
73738714:73738714(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.84C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |