Variant #0000724622 (NC_000014.8:g.102898460_102898462dup, NM_014844.3:c.1412_1414dup (TECPR2))

Chromosome 14
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.102898460_102898462dup
DNA change (hg38) -
Published as TECPR2(NM_014844.4):c.1412_1414dupAGA (p.K471dup)
ISCN -
DB-ID CINP_000003
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TECPR2 NM_014844.3 ?/. - c.1412_1414dup r.(?) p.(Lys471dup)
CINP NM_032630.2 ?/. - c.-69257_-69255dup r.(?) p.(=)


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