| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309784 |
| Start |
160438512:160438512(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.672A>T |
| AA Mutation |
p.Arg224Ser(p.R224S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309784 |
| Start |
160438166:160438166(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1018G>C |
| AA Mutation |
p.Val340Leu(p.V340L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309784 |
| Start |
160439010:160439010(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.174T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |