Variant #0000515429 (NC_000002.11:g.25016120G>T, NM_004036.3:c.*26681C>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.25016120G>T
DNA change (hg38) g.24793251G>T
Published as PTRHD1(NM_001013663.1):c.127C>A (p.P43T)
ISCN -
DB-ID ADCY3_000009
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) 0.00218 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.127C>A r.(?) p.(Pro43Thr)
ADCY3 NM_004036.3 -/. - c.*26681C>A r.(=) p.(=)
CENPO NM_024322.2 -/. - c.-338G>T r.(?) p.(=)


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