| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343090 |
| Start |
10161174:10161174(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3086T>C |
| AA Mutation |
p.Met1029Thr(p.M1029T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343090 |
| Start |
10135147:10135147(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2185G>C |
| AA Mutation |
p.Ala729Pro(p.A729P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343090 |
| Start |
10137147:10137147(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761724316
|
| CDS Mutation |
c.2305A>G |
| AA Mutation |
p.Ile769Val(p.I769V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |