Variant #0000533499 (NC_000008.10:g.106431420A>G, NM_012082.3:c.89A>G (ZFPM2))

Chromosome 8
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.106431420A>G
DNA change (hg38) g.105419192A>G
Published as ZFPM2(NM_012082.3):c.89A>G (p.(Glu30Gly)), ZFPM2(NM_012082.4):c.89A>G (p.E30G)
ISCN -
DB-ID ZFPM2_000013 See all 6 reported entries
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) 0.00268 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +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     
ZFPM2 NM_012082.3 -/. - c.89A>G r.(?) p.(Glu30Gly)


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