| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358171 |
| Start |
75566789:75566789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.440T>A |
| AA Mutation |
p.Val147Glu(p.V147E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358171 |
| Start |
75569144:75569144(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.927T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358171 |
| Start |
75572047:75572047(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1221C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |