| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295101 |
| Start |
154855024:154855024(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1217T>A |
| AA Mutation |
p.Ile406Asn(p.I406N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000295101 |
| Start |
154854729:154854729(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.922A>G |
| AA Mutation |
p.Met308Val(p.M308V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295101 |
| Start |
154699329:154699329(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.554C>A |
| AA Mutation |
p.Ser185Tyr(p.S185Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |