Variant #0000244027 (NC_000003.11:g.87381765A>C, NM_014043.3:c.(372A>C) (CHMP2B))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.87381765A>C
DNA change (hg38) g.87332615A>C
Published as -
ISCN -
DB-ID CHMP2B_000012 See all 3 reported entries
Variant remarks Corresponds to SNP <a href=\""http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?rs=1044499"""" target=""""_blank"""">rs1044499</a>. /r/Silent point mutation in coding region""
Reference -
ClinVar ID -
dbSNP ID rs1044499
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Marc Cruts
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-05-01 13:44:57 +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     
CHMP2B NM_014043.3 -/? 4 c.(372A>C) r.(?) p.(=)


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