| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340748 |
| Start |
10140888:10140888(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3368A>C |
| AA Mutation |
p.Gln1123Pro(p.Q1123P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000340748 |
| Start |
10137928:10137928(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764029022
|
| CDS Mutation |
c.4149A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000340748 |
| Start |
10175619:10175619(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.522-1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |