Variant #0000248832 (NC_000001.10:g.114438951A>G, NM_006594.3:c.1439T>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.114438951A>G
DNA change (hg38) g.113896329A>G
Published as AP4B1(NM_006594.5):c.1439T>C (p.L480S), AP4B1-AS1(NR_037864.1):n.247-1539A>G
ISCN -
DB-ID AP4B1_000008
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) 0.30318 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.-8954T>C r.(?) p.(=)
AP4B1 NM_006594.3 -/. - c.1439T>C r.(?) p.(Leu480Ser)
PTPN22 NM_015967.5 -/. - c.-24706T>C r.(?) p.(=)
AP4B1-AS1 NR_037864.1 -/. - n.247-1539A>G r.(?) -


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