| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369850 |
| Start |
154354896:154354896(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.5146C>A |
| AA Mutation |
p.Gln1716Lys(p.Q1716K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369850 |
| Start |
154367414:154367414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.851C>T |
| AA Mutation |
p.Ala284Val(p.A284V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369850 |
| Start |
154357578:154357578(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4801G>A |
| AA Mutation |
p.Asp1601Asn(p.D1601N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |