Variant #0000990125 (NC_000001.10:g.114401177C>G, NM_006594.3:c.*36510G>C (AP4B1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.114401177C>G
DNA change (hg38) -
Published as PTPN22(NM_015967.8):c.292G>C (p.A98P)
ISCN -
DB-ID AP4B1_000074
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) 1.0E-5 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 2024-08-28 13:07:21 +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.*22568G>C r.(=) p.(=)
AP4B1 NM_006594.3 ?/. - c.*36510G>C r.(=) p.(=)
PTPN22 NM_015967.5 ?/. - c.292G>C r.(?) p.(Ala98Pro)
AP4B1-AS1 NR_037864.1 ?/. - n.246+539C>G r.(?) -


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