Variant #0000928573 (NC_000002.11:g.25046216A>G, NM_004036.3:c.2745T>C (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.25046216A>G
DNA change (hg38) -
Published as ADCY3(NM_001377128.1):c.2811T>C (p.Y937=)
ISCN -
DB-ID ADCY3_000033
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +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     
PTRHD1 NM_001013663.1 -?/. - c.-29970T>C r.(?) p.(=)
ADCY3 NM_004036.3 -?/. - c.2745T>C r.(?) p.(=)
CENPO NM_024322.2 -?/. - c.*4029A>G r.(=) p.(=)


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