Variant #0000800534 (NC_000002.11:g.25043645G>A, NM_004036.3:c.3200C>T (ADCY3))

Chromosome 2
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.25043645G>A
DNA change (hg38) -
Published as ADCY3(NM_001320613.1):c.3203C>T (p.T1068I)
ISCN -
DB-ID ADCY3_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.-27399C>T r.(?) p.(=)
ADCY3 NM_004036.3 ?/. - c.3200C>T r.(?) p.(Thr1067Ile)
CENPO NM_024322.2 ?/. - c.*1458G>A r.(=) p.(=)


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