Variant #0001000684 (NC_000014.8:g.102964008G>A, NM_014844.3:c.4033G>A (TECPR2))

Chromosome 14
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.102964008G>A
DNA change (hg38) -
Published as TECPR2(NM_014844.5):c.4033G>A (p.A1345T)
ISCN -
DB-ID CINP_000019
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) 0.00089 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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     
TECPR2 NM_014844.3 -/. - c.4033G>A r.(?) p.(Ala1345Thr)
CINP NM_032630.2 -/. - c.-134820C>T r.(?) p.(=)


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