Variant #0000261130 (NC_000005.9:g.115177207T>C, NM_001284.2:c.-528T>C (AP3S1))

Chromosome 5
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.115177207T>C
DNA change (hg38) g.115841510T>C
Published as ATG12(NM_004707.4):c.43A>G (p.I15V)
ISCN -
DB-ID ATG12_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) 0.01742 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP3S1 NM_001284.2 -/. - c.-528T>C r.(?) p.(=)
ATG12 NM_004707.3 -/. - c.43A>G r.(?) p.(Ile15Val)


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