Variant #0000712964 (NC_000011.9:g.19209751G>A, NM_003476.4:c.213C>T (CSRP3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19209751G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CSRP3_000094 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs45476991
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00496 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-01-25 12:13:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +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.213C>T r.(?) p.(Ile71=)


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