| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260187 |
| Start |
119357565:119357565(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1527G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260187 |
| Start |
119373034:119373034(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.447T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000260187 |
| Start |
119372992:119372997(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.484_489delGACCCC |
| AA Mutation |
p.Asp162_Pro163del(p.D162_P163del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |