| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299766 |
| Start |
60371890:60371890(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.460G>T |
| AA Mutation |
p.Ala154Ser(p.A154S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000299766 |
| Start |
60372101:60372101(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.249C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000299766 |
| Start |
60371897:60371897(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142925940
|
| CDS Mutation |
c.453C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |