| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298048 |
| Start |
36630342:36630342(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.710T>G |
| AA Mutation |
p.Ile237Ser(p.I237S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298048 |
| Start |
36630341:36630341(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.709A>G |
| AA Mutation |
p.Ile237Val(p.I237V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298048 |
| Start |
36589549:36589549(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.158G>T |
| AA Mutation |
p.Arg53Leu(p.R53L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |