Variant #0000885090 (NC_000002.11:g.25061488G>A, NM_004036.3:c.1359C>T (ADCY3))

Chromosome 2
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.25061488G>A
DNA change (hg38) -
Published as ADCY3(NM_001320613.2):c.1359C>T (p.R453=)
ISCN -
DB-ID ADCY3_000022
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +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     
ADCY3 NM_004036.3 -?/. - c.1359C>T r.(?) p.(Arg453=)
CENPO NM_024322.2 -?/. - c.*19301G>A r.(=) p.(=)


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