| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265560 |
| Start |
49327747:49327747(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.299C>G |
| AA Mutation |
p.Ala100Gly(p.A100G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265560 |
| Start |
49278894:49278894(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2653T>C |
| AA Mutation |
p.Tyr885His(p.Y885H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265560 |
| Start |
49284127:49284127(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2400C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |