Variant #0000678268 (NC_000008.10:g.106814597G>A, NM_012082.3:c.2287G>A (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.106814597G>A
DNA change (hg38) -
Published as ZFPM2(NM_001362837.1):c.1891G>A (p.V631I), ZFPM2(NM_012082.3):c.2287G>A (p.V763I, p.(Val763Ile)), ZFPM2(NM_012082.4):c.2287G>A (p.V763I)
ISCN -
DB-ID ZFPM2_000035 See all 4 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +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.2287G>A r.(?) p.(Val763Ile)


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