| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256103 |
| Start |
81444562:81444562(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.286C>A |
| AA Mutation |
p.Gln96Lys(p.Q96K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256103 |
| Start |
81444960:81444960(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.103A>G |
| AA Mutation |
p.Asn35Asp(p.N35D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256103 |
| Start |
81444871:81444871(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.192C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |