| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000313375 |
| Start |
73597705:73597705(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782298020
|
| CDS Mutation |
c.1080C>G |
| AA Mutation |
p.Asn360Lys(p.N360K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000313375 |
| Start |
73593937:73593937(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2487G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000313375 |
| Start |
73616075:73616075(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.396C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |