Variant #0000543406 (NC_000011.9:g.19209833A>G, NM_003476.4:c.131T>C (CSRP3))

Chromosome 11
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.19209833A>G
DNA change (hg38) g.19188286A>G
Published as CSRP3(NM_003476.3):c.131T>C (p.L44P), CSRP3(NM_003476.5):c.131T>C (p.L44P)
ISCN -
DB-ID CSRP3_000043 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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSRP3 NM_003476.4 +?/. - c.131T>C r.(?) p.(Leu44Pro)


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