| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000275815 |
| Start |
143399701:143399701(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.785G>A |
| AA Mutation |
p.Cys262Tyr(p.C262Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000275815 |
| Start |
143394856:143394856(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2304T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000275815 |
| Start |
143401507:143401507(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.249C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |