| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000354667 |
| Start |
26197645:26197645(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.130T>G |
| AA Mutation |
p.Trp44Gly(p.W44G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000354667 |
| Start |
26193288:26193288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774142726
|
| CDS Mutation |
c.963T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000354667 |
| Start |
26193318:26193320(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.931_933delTCT |
| AA Mutation |
p.Ser311del(p.S311del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |