| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000515384 |
| Start |
25169788:25169788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1832G>C |
| AA Mutation |
p.Ser611Thr(p.S611T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000515384 |
| Start |
25171120:25171120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.500T>C |
| AA Mutation |
p.Leu167Pro(p.L167P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000515384 |
| Start |
25170120:25170120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1500C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |