Variant #0000567828 (NC_000019.9:g.47259134C>A, NM_024301.4:c.427C>A (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47259134C>A
DNA change (hg38) g.46755877C>A
Published as FKRP(NM_001039885.2):c.427C>A (p.R143S, p.(Arg143Ser)), FKRP(NM_001039885.3):c.427C>A (p.R143S), FKRP(NM_024301.5):c.427C>A (p.R143S)
ISCN -
DB-ID FKRP_000007 See all 27 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) 0.0045 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.-9447G>T r.(?) p.(=)
SLC1A5 NM_001145144.1 -?/. - c.*19633G>T r.(=) p.(=)
FKRP NM_024301.4 -?/. - c.427C>A r.(?) p.(Arg143Ser)


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