Variant #0000689099 (NC_000003.11:g.47458623G>C, NM_015466.2:c.*3948G>C (PTPN23))

Chromosome 3
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.47458623G>C
DNA change (hg38) -
Published as SCAP(NM_012235.4):c.3045C>G (p.F1015L)
ISCN -
DB-ID PTPN23_000016
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) 5.0E-5 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 2020-09-15 15:50:26 +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     
SCAP NM_012235.2 -?/. - c.3045C>G r.(?) p.(Phe1015Leu)
PTPN23 NM_015466.2 -?/. - c.*3948G>C r.(=) p.(=)


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