Variant #0000551241 (NC_000014.8:g.102843158A>G, NM_014844.3:c.100A>G (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.102843158A>G
DNA change (hg38) g.102376821A>G
Published as TECPR2(NM_014844.3):c.100A>G (p.(Ile34Val)), TECPR2(NM_014844.4):c.100A>G (p.I34V)
ISCN -
DB-ID TECPR2_000022 See all 2 reported entries
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TECPR2 NM_014844.3 -?/. - c.100A>G r.(?) p.(Ile34Val)
CINP NM_032630.2 -?/. - c.-13970T>C r.(?) p.(=)


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