| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361138 |
| Start |
70259139:70259139(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.61C>G |
| AA Mutation |
p.Pro21Ala(p.P21A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361138 |
| Start |
70323493:70323493(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2161A>T |
| AA Mutation |
p.Met721Leu(p.M721L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361138 |
| Start |
70264379:70264379(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.261G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |