Variant #0000886289 (NC_000004.11:g.44700615A>G, NM_021927.2:c.1927A>G (GUF1))

Chromosome 4
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.44700615A>G
DNA change (hg38) -
Published as GUF1(NM_001345867.1):c.955A>G (p.K319E)
ISCN -
DB-ID GNPDA2_000003
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GUF1 NM_021927.2 ?/. - c.1927A>G r.(?) p.(Lys643Glu)
GNPDA2 NM_138335.2 ?/. - c.*4483T>C r.(=) p.(=)


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