| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000325680 |
| Start |
74763807:74763807(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.318G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000325680 |
| Start |
74809627:74809629(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4769_4771delGAC |
| AA Mutation |
p.Gly1590_Leu1591delinsVal(p.G1590_L1591delinsV) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000325680 |
| Start |
74781646:74781654(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1603_1611delCCTCCAGTG |
| AA Mutation |
p.Pro535_Val537del(p.P535_V537del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |