Variant #0001004909 (NC_000019.9:g.47259605G>A, NM_024301.4:c.898G>A (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47259605G>A
DNA change (hg38) -
Published as FKRP(NM_001039885.2):c.898G>A (p.(Val300Met)), FKRP(NM_024301.5):c.898G>A (p.V300M)
ISCN -
DB-ID FKRP_000051 See all 7 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +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.-9918C>T r.(?) p.(=)
SLC1A5 NM_001145144.1 +?/. - c.*19162C>T r.(=) p.(=)
FKRP NM_024301.4 +?/. - c.898G>A r.(?) p.(Val300Met)


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