Variant #0000567818 (NC_000019.9:g.47258942G>A, NM_024301.4:c.235G>A (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.47258942G>A
DNA change (hg38) g.46755685G>A
Published as FKRP(NM_001039885.2):c.235G>A (p.(Val79Met)), FKRP(NM_001039885.3):c.235G>A (p.V79M)
ISCN -
DB-ID FKRP_000063 See all 9 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00099 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRN4 NM_001039877.1 -/. - c.-9255C>T r.(?) p.(=)
SLC1A5 NM_001145144.1 -/. - c.*19825C>T r.(=) p.(=)
FKRP NM_024301.4 -/. - c.235G>A r.(?) p.(Val79Met)


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