Variant #0000680304 (NC_000015.9:g.80873642C>G, NM_014862.3:c.1815C>G (ARNT2))

Chromosome 15
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.80873642C>G
DNA change (hg38) -
Published as ARNT2(NM_014862.3):c.1815C>G (p.(=)), ARNT2(NM_014862.4):c.1815C>G (p.T605=)
ISCN -
DB-ID ARNT2_000007 See all 2 reported entries
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) 0.03993 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARNT2 NM_014862.3 -?/. - c.1815C>G r.(?) p.(Thr605=)


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