Variant #0000502947 (NC_000001.10:g.144881444T>C, NM_022359.5:c.*70753A>G (PDE4DIP))

Chromosome 1
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.144881444T>C
DNA change (hg38) g.149003028A>G
Published as PDE4DIP(NM_014644.5):c.3752A>G (p.Y1251C)
ISCN -
DB-ID PDE4DIP_000006
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_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 2020-06-23 18:43:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4DIP NM_014644.5 ?/. - c.3752A>G r.(?) p.(Tyr1251Cys)
PDE4DIP NM_022359.5 ?/. - c.*70753A>G r.(=) p.(=)


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