Variant #0000326657 (NC_000019.9:g.47260091C>T, NM_024301.4:c.1384C>T (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47260091C>T
DNA change (hg38) g.46756834C>T
Published as FKRP(NM_001039885.2):c.1384C>T (p.(Pro462Ser)), FKRP(NM_001039885.3):c.1384C>T (p.P462S)
ISCN -
DB-ID FKRP_000037 See all 16 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRN4 NM_001039877.1 +/. - c.-10404G>A r.(?) p.(=)
SLC1A5 NM_001145144.1 +/. - c.*18676G>A r.(=) p.(=)
FKRP NM_024301.4 +/. - c.1384C>T r.(?) p.(Pro462Ser)


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