| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265171 |
| Start |
109980020:109980020(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2102A>G |
| AA Mutation |
p.Asp701Gly(p.D701G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265171 |
| Start |
109983517:109983517(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2467C>A |
| AA Mutation |
p.Leu823Ile(p.L823I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265171 |
| Start |
109994755:109994755(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2880C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |