Variant #0000983500 (NC_000019.9:g.42799176G>T, NM_015125.3:c.4660G>T (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.42799176G>T
DNA change (hg38) -
Published as CIC(NM_001386298.1):c.7387G>T (p.(Ala2463Ser))
ISCN -
DB-ID CIC_000117
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
CIC NM_001386298.1 -?/. - c.7387G>T r.(?) p.(Ala2463Ser)
PAFAH1B3 NM_002573.3 -?/. - c.*2054C>A r.(=) p.(=)
CIC NM_015125.3 -?/. - c.4660G>T r.(?) p.(Ala1554Ser)
PRR19 NM_199285.2 -?/. - c.-7486G>T r.(?) p.(=)


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