Variant #0000337025 (NC_000001.10:g.114443035C>G, NC_000001.10(NM_006594.3):c.618-13G>C (AP4B1))

Chromosome 1
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.114443035C>G
DNA change (hg38) g.113900413C>G
Published as AP4B1(NM_006594.5):c.618-13G>C, AP4B1-AS1(NR_037864.1):n.910C>G
ISCN -
DB-ID AP4B1_000013 See all 2 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) 0.38578 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
BCL2L15 NM_001010922.2 -/. - c.-13038G>C r.(?) p.(=)
AP4B1 NM_006594.3 -/. - c.618-13G>C r.(=) p.(=)
PTPN22 NM_015967.5 -/. - c.-28790G>C r.(?) p.(=)
DCLRE1B NM_022836.3 -/. - c.-5174C>G r.(?) p.(=)
AP4B1-AS1 NR_037864.1 -/. - n.910C>G r.(?) -


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