Variant #0000299928 (NC_000001.10:g.160319972G>A, NM_004371.3:c.-7012C>T (COPA))

Chromosome 1
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.160319972G>A
DNA change (hg38) g.160350182G>A
Published as NCSTN(NM_015331.3):c.514G>A (p.A172T)
ISCN -
DB-ID NCSTN_000008
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COPA NM_004371.3 ?/. - c.-7012C>T r.(?) p.(=)
NCSTN NM_015331.2 ?/. - c.514G>A r.(?) p.(Ala172Thr)


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