| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000293897 |
| Start |
1079612:1079612(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.744C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000293897 |
| Start |
1079924:1079924(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774838845
|
| CDS Mutation |
c.1056C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
inframe_insertion |
| Transcription ID |
ENST00000293897 |
| Start |
1079139:1079140(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.273_274insTTG |
| AA Mutation |
p.Leu91dup(p.L91dup) |
| Mutation Classification |
In_Frame_Ins |
| Feature Type |
Transcript |