| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285879 |
| Start |
141905540:141905540(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.136G>C |
| AA Mutation |
p.Asp46His(p.D46H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285879 |
| Start |
141906790:141906790(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1386C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285879 |
| Start |
141907210:141907210(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1806G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |