| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371793 |
| Start |
135119840:135119840(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1120G>A |
| AA Mutation |
p.Ala374Thr(p.A374T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000371793 |
| Start |
135098287:135098287(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs367620749
|
| CDS Mutation |
c.458C>T |
| AA Mutation |
p.Ala153Val(p.A153V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371793 |
| Start |
135106846:135106846(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs557820013
|
| CDS Mutation |
c.774C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |