Variant #0000547302 (NC_000012.11:g.15731724_15731725insG, NC_000012.11(NM_002848.3):c.2746-63_2746-62insG (PTPRO))

Chromosome 12
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.15731724_15731725insG
DNA change (hg38) g.15578790_15578791insG
Published as PTPRO(NM_030667.3):c.2830-63_2830-62insG
ISCN -
DB-ID PTPRO_000022
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPRO NM_002848.3 -/. - c.2746-63_2746-62insG r.(=) p.(=)


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