Variant #0000870318 (NC_000002.11:g.29294528G>A, NM_001029883.2:c.2600C>T (C2orf71))

Chromosome 2
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.29294528G>A
DNA change (hg38) -
Published as c.2600C>T
ISCN -
DB-ID C2orf71_000006 See all 10 reported entries
Variant remarks -
Reference PubMed: Audo 2011
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency 1/418 patient homozygous for this variant patient chromosomes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00194 View details
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2022-06-18 03:05:08 +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     
C2orf71 NM_001029883.2 -?/. 1 c.2600C>T r.(?) p.(Pro867Leu)


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