Variant #0000532175 (NC_000007.13:g.4824629G>A, NM_014855.2:c.881G>A (AP5Z1))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4824629G>A
DNA change (hg38) g.4784998G>A
Published as AP5Z1(NM_014855.2):c.881G>A (p.(Arg294Gln)), AP5Z1(NM_014855.3):c.881G>A (p.R294Q)
ISCN -
DB-ID AP5Z1_000010 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) 0.00316 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP5Z1 NM_014855.2 -?/. - c.881G>A r.(?) p.(Arg294Gln)


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