Variant #0000551271 (NC_000014.8:g.102912150C>A, NM_014844.3:c.2941C>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.102912150C>A
DNA change (hg38) g.102445813C>A
Published as TECPR2(NM_014844.4):c.2941C>A (p.Q981K), TECPR2(NM_014844.5):c.2941C>A (p.Q981K)
ISCN -
DB-ID TECPR2_000004 See all 3 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) 0.01734 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TECPR2 NM_014844.3 -/. - c.2941C>A r.(?) p.(Gln981Lys)
CINP NM_032630.2 -/. - c.-82962G>T r.(?) p.(=)


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