Variant #0000798679 (NC_000001.10:g.114441334C>T, NC_000001.10(NM_006594.3):c.1198+6G>A (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.114441334C>T
DNA change (hg38) -
Published as AP4B1(NM_006594.4):c.1198+6G>A
ISCN -
DB-ID AP4B1_000062
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 -?/. - c.-11337G>A r.(?) p.(=)
AP4B1 NM_006594.3 -?/. - c.1198+6G>A r.(=) p.(=)
PTPN22 NM_015967.5 -?/. - c.-27089G>A r.(?) p.(=)
AP4B1-AS1 NR_037864.1 -?/. - n.368+723C>T r.(?) -


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