| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358252 |
| Start |
57309430:57309430(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3281T>C |
| AA Mutation |
p.Val1094Ala(p.V1094A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358252 |
| Start |
57300889:57300889(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.5124C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358252 |
| Start |
57309858:57309858(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2853G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |