Variant #0000806246 (NC_000014.8:g.102900831T>C, NM_014844.3:c.1677T>C (TECPR2))

Chromosome 14
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.102900831T>C
DNA change (hg38) -
Published as TECPR2(NM_014844.4):c.1677T>C (p.S559=)
ISCN -
DB-ID CINP_000006
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) 6.0E-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 2021-09-17 14:40:49 +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.1677T>C r.(?) p.(Ser559=)
CINP NM_032630.2 -?/. - c.-71643A>G r.(?) p.(=)


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