Variant #0000288319 (NC_000017.10:g.17942806G>A, NM_145691.3:c.-479C>T (ATPAF2))

Chromosome 17
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.17942806G>A
DNA change (hg38) g.18039492G>A
Published as GID4(NM_024052.4):c.28G>A (p.G10R)
ISCN -
DB-ID GID4_000001
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 2018-01-15 20:58:59 +01:00 (CET)
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     
GID4 NM_024052.4 ?/. - c.28G>A r.(?) p.(Gly10Arg)
ATPAF2 NM_145691.3 ?/. - c.-479C>T r.(?) p.(=)


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