| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394518 |
| Start |
85580939:85580939(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2871A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000394518 |
| Start |
85580940:85580940(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2872C>T |
| AA Mutation |
p.Gln958Ter(p.Q958*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000394518 |
| Start |
85581673:85581673(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3605C>G |
| AA Mutation |
p.Ser1202Ter(p.S1202*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |