| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000409785 |
| Start |
85049433:85049433(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747547909
|
| CDS Mutation |
c.669C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000409785 |
| Start |
85049523:85049523(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs11554335
|
| CDS Mutation |
c.759C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000409785 |
| Start |
85028002:85028010(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.134_142delGGCATACAA |
| AA Mutation |
p.Arg45_Thr47del(p.R45_T47del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |