Variant #0000505114 (NC_000001.10:g.214557062_214557067del, NM_005401.4:c.2144_2149del (PTPN14))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.214557062_214557067del
DNA change (hg38) g.214383719_214383724del
Published as PTPN14(NM_005401.4):c.2144_2149delAGGAGG (p.E715_E716del)
ISCN -
DB-ID PTPN14_000028
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPN14 NM_005401.4 -/. - c.2144_2149del r.(?) p.(Glu715_Glu716del)


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