Variant #0000808961 (NC_000019.9:g.47260112C>T, NM_024301.4:c.1405C>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.47260112C>T
DNA change (hg38) -
Published as FKRP(NM_001039885.3):c.1405C>T (p.L469=)
ISCN -
DB-ID FKRP_000082 See all 2 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) 0.00018 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRN4 NM_001039877.1 -/. - c.-10425G>A r.(?) p.(=)
SLC1A5 NM_001145144.1 -/. - c.*18655G>A r.(=) p.(=)
FKRP NM_024301.4 -/. - c.1405C>T r.(?) p.(Leu469=)


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