| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295566 |
| Start |
155659941:155659941(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2107C>T |
| AA Mutation |
p.Pro703Ser(p.P703S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000295566 |
| Start |
155679438:155679439(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.293_294delAA |
| AA Mutation |
p.Gln98ArgfsTer2(p.Q98Rfs*2) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000295566 |
| Start |
155679436:155679437(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.295_296insTC |
| AA Mutation |
p.Ala99ValfsTer20(p.A99Vfs*20) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |