Variant #0000951173 (NC_000019.9:g.10206662T>C, NM_031917.2:c.578A>G (ANGPTL6))

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.10206662T>C
DNA change (hg38) -
Published as ANGPTL6(NM_031917.3):c.578A>G (p.Q193R)
ISCN -
DB-ID ANGPTL6_000004
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) 0.0006 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     
C19orf66 NM_018381.2 ?/. - c.*3684T>C r.(=) p.(=)
ANGPTL6 NM_031917.2 ?/. - c.578A>G r.(?) p.(Gln193Arg)


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