Variant #0000502536 (NC_000001.10:g.114372214C>G, NM_015967.5:c.2250G>C (PTPN22))

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.114372214C>G
DNA change (hg38) g.113829592C>G
Published as PTPN22(NM_015967.6):c.2250G>C (p.K750N), PTPN22(NM_015967.8):c.2250G>C (p.K750N)
ISCN -
DB-ID PTPN22_000003 See all 4 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) 0.00596 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 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPN22 NM_015967.5 -?/. - c.2250G>C r.(?) p.(Lys750Asn)


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