Variant #0000567521 (NC_000019.9:g.42799051G>A, NM_015125.3:c.4535G>A (CIC))

Chromosome 19
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.42799051G>A
DNA change (hg38) g.42294899G>A
Published as CIC(NM_001304815.1):c.7262G>A (p.R2421H)
ISCN -
DB-ID CIC_000039
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAFAH1B3 NM_002573.3 ?/. - c.*2179C>T r.(=) p.(=)
CIC NM_015125.3 ?/. - c.4535G>A r.(?) p.(Arg1512His)
PRR19 NM_199285.2 ?/. - c.-7611G>A r.(?) p.(=)


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