Variant #0000543408 (NC_000011.9:g.19213898G>A, NM_003476.4:c.98C>T (CSRP3))

Chromosome 11
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.19213898G>A
DNA change (hg38) g.19192351G>A
Published as CSRP3(NM_003476.3):c.98C>T (p.T33M), CSRP3(NM_003476.5):c.98C>T (p.T33M)
ISCN -
DB-ID CSRP3_000072 See all 4 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSRP3 NM_003476.4 ?/. - c.98C>T r.(?) p.(Thr33Met)


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