Variant #0000241122 (NC_000019.9:g.47251688C>T, NC_000019.9(NM_024301.4):c.-190-84C>T (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47251688C>T
DNA change (hg38) g.46748431C>T
Published as -
ISCN -
DB-ID FKRP_000049
Variant remarks -
Reference rs1644332
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2004-12-17 17:36:24 +01:00 (CET)
Date last edited 2012-11-02 20:42:36 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKRP NM_024301.4 -/. 3 c.-190-84C>T r.(?) p.(=)


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