Variant #0000692813 (NC_000019.9:g.42797227T>C, NM_015125.3:c.3589T>C (CIC))

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.42797227T>C
DNA change (hg38) -
Published as CIC(NM_001304815.1):c.6316T>C (p.S2106P)
ISCN -
DB-ID CIC_000063
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAFAH1B3 NM_002573.3 -?/. - c.*4003A>G r.(=) p.(=)
CIC NM_015125.3 -?/. - c.3589T>C r.(?) p.(Ser1197Pro)
PRR19 NM_199285.2 -?/. - c.-9435T>C r.(?) p.(=)


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