Variant #0000251908 (NC_000001.10:g.160322970A>C, NM_004371.3:c.-10010T>G (COPA))

Chromosome 1
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.160322970A>C
DNA change (hg38) g.160353180A>C
Published as NCSTN(NM_015331.3):c.1122A>C (p.L374F)
ISCN -
DB-ID NCSTN_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) 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.-10010T>G r.(?) p.(=)
NCSTN NM_015331.2 -?/. - c.1122A>C r.(?) p.(Leu374Phe)


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