Variant #0000287538 (NC_000019.9:g.47259163C>G, NM_024301.4:c.456C>G (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47259163C>G
DNA change (hg38) g.46755906C>G
Published as FKRP(NM_001039885.2):c.456C>G (p.S152R, p.(Ser152Arg)), FKRP(NM_001039885.3):c.456C>G (p.S152R), FKRP(NM_024301.5):c.456C>G (p.S152R)
ISCN -
DB-ID FKRP_000095 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) 0.00049 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.-9476G>C r.(?) p.(=)
SLC1A5 NM_001145144.1 ?/. - c.*19604G>C r.(=) p.(=)
FKRP NM_024301.4 ?/. - c.456C>G r.(?) p.(Ser152Arg)


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