Variant #0000951310 (NC_000019.9:g.42796277G>A, NM_015125.3:c.2926G>A (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.42796277G>A
DNA change (hg38) -
Published as CIC(NM_015125.5):c.2926G>A (p.G976S)
ISCN -
DB-ID CIC_000109
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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     
CIC NM_001386298.1 -?/. - c.5653G>A r.(?) p.(Gly1885Ser)
PAFAH1B3 NM_002573.3 -?/. - c.*4953C>T r.(=) p.(=)
CIC NM_015125.3 -?/. - c.2926G>A r.(?) p.(Gly976Ser)
PRR19 NM_199285.2 -?/. - c.-10385G>A r.(?) p.(=)


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