Variant #0000244084 (NC_000016.9:g.31103913G>A, NM_004960.3:c.(676G>A) (FUS))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31103913G>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
FUS_000112 |
Variant remarks |
Observed in 1 control, not in ALS patients. /r/Point mutation in coding region predicting an amino acid substitution Variant Error [EREF/EUNCERTAIN]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message. |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Marc Cruts |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2013-05-01 13:44:57 +02:00 (CEST) |
Date last edited |
2019-07-16 18:35:02 +02:00 (CEST) |

Variant on transcripts
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