Variant #0000688722 (NC_000002.11:g.25013426C>T, NM_004036.3:c.*29375G>A (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.25013426C>T
DNA change (hg38) -
Published as PTRHD1(NM_001013663.2):c.277G>A (p.E93K)
ISCN -
DB-ID ADCY3_000012
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTRHD1 NM_001013663.1 ?/. - c.277G>A r.(?) p.(Glu93Lys)
ADCY3 NM_004036.3 ?/. - c.*29375G>A r.(=) p.(=)
CENPO NM_024322.2 ?/. - c.-3032C>T r.(?) p.(=)


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