| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155168593:155168593(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1882A>C |
| AA Mutation |
p.Asn628His(p.N628H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155172146:155172146(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2010C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000360490 |
| Start |
155172213:155172213(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2076+1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |