Variant #0000947812 (NC_000002.11:g.25048974C>T, NM_004036.3:c.2517G>A (ADCY3))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25048974C>T
DNA change (hg38) -
Published as ADCY3(NM_001377128.1):c.2583G>A (p.K861=)
ISCN -
DB-ID ADCY3_000038
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 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 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     
PTRHD1 NM_001013663.1 -/. - c.-32728G>A r.(?) p.(=)
ADCY3 NM_004036.3 -/. - c.2517G>A r.(?) p.(=)
CENPO NM_024322.2 -/. - c.*6787C>T r.(=) p.(=)


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