| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000231656 |
| Start |
150166922:150166922(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.46G>A |
| AA Mutation |
p.Gly16Ser(p.G16S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000231656 |
| Start |
150183549:150183549(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.667C>T |
| AA Mutation |
p.Pro223Ser(p.P223S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000231656 |
| Start |
150166924:150166924(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.48C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |