Variant #0000617648 (NC_000019.9:g.42799323A>C, NM_015125.3:c.4807A>C (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.42799323A>C
DNA change (hg38) g.42295171A>C
Published as CIC(NM_015125.3):c.4807A>C (p.(Thr1603Pro))
ISCN -
DB-ID CIC_000048
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 2019-12-04 15:24:38 +01:00 (CET)
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.*1907T>G r.(=) p.(=)
CIC NM_015125.3 ?/. - c.4807A>C r.(?) p.(Thr1603Pro)
PRR19 NM_199285.2 ?/. - c.-7339A>C r.(?) p.(=)


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