Variant #0000502554 (NC_000001.10:g.114442885A>G, NM_006594.3:c.755T>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.114442885A>G
DNA change (hg38) g.113900263A>G
Published as AP4B1(NM_006594.4):c.755T>C (p.V252A), AP4B1(NM_006594.5):c.755T>C (p.V252A)
ISCN -
DB-ID AP4B1_000033 See all 3 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) 0.00115 View details
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 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 -?/. - c.-12888T>C r.(?) p.(=)
AP4B1 NM_006594.3 -?/. - c.755T>C r.(?) p.(Val252Ala)
PTPN22 NM_015967.5 -?/. - c.-28640T>C r.(?) p.(=)
DCLRE1B NM_022836.3 -?/. - c.-5324A>G r.(?) p.(=)
AP4B1-AS1 NR_037864.1 -?/. - n.760A>G r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.