| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260947 |
| Start |
214781422:214781422(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.452G>A |
| AA Mutation |
p.Ser151Asn(p.S151N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260947 |
| Start |
214809555:214809555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.15G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260947 |
| Start |
214792318:214792318(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.343C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |