Variant #0000656844 (NC_000011.9:g.64977937A>G, NC_000011.9(NM_005186.3):c.2059+14A>G (CAPN1))

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.64977937A>G
DNA change (hg38) g.65210466A>G
Published as -
ISCN -
DB-ID SLC22A20_000004
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) 0.76244 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A20 NM_001004326.4 -/. - c.-3407A>G r.(?) p.(=)
CAPN1 NM_005186.3 -/. - c.2059+14A>G r.(=) p.(=)


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