Variant #0001052056 (NC_000005.9:g.115202418A>G, NM_001284.2:c.121A>G (AP3S1))

Chromosome 5
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.115202418A>G
DNA change (hg38) -
Published as AP3S1(NM_001284.4):c.121A>G (p.(Lys41Glu))
ISCN -
DB-ID AP3S1_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP3S1 NM_001284.2 ?/. - c.121A>G r.(?) p.(Lys41Glu)
ATG12 NM_004707.3 ?/. - c.-25169T>C r.(?) p.(=)


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