Variant #0000989359 (NC_000009.11:g.95481441G>A, NM_001003800.1:c.1486C>T (BICD2))

Chromosome 9
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.95481441G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID BICD2_000071
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1457844438
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-03 17:10:01 +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     
BICD2 NM_001003800.1 ?/. - c.1486C>T r.(?) p.(Arg496Cys)


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