| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000575354 |
| Start |
42294994:42294994(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770823747
|
| CDS Mutation |
c.4630G>A |
| AA Mutation |
p.Ala1544Thr(p.A1544T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000575354 |
| Start |
42293038:42293038(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3552C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000575354 |
| Start |
42290934:42290934(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2166G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |