Variant #0000502561 (NC_000001.10:g.114453877A>G, NM_006594.3:c.-6390T>C (AP4B1))

Chromosome 1
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.114453877A>G
DNA change (hg38) g.113911255A>G
Published as DCLRE1B(NM_022836.4):c.663A>G (p.T221=)
ISCN -
DB-ID AP4B1_000040
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP4B1 NM_006594.3 -?/. - c.-6390T>C r.(?) p.(=)
DCLRE1B NM_022836.3 -?/. - c.663A>G r.(?) p.(Thr221=)


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