Variant #0000538689 (NC_000009.11:g.95491490T>C, NM_001003800.1:c.269A>G (BICD2))

Chromosome 9
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.95491490T>C
DNA change (hg38) g.92729208T>C
Published as BICD2(NM_001003800.1):c.269A>G (p.(Lys90Arg)), BICD2(NM_001003800.2):c.269A>G (p.K90R), BICD2(NM_015250.4):c.269A>G (p.K90R)
ISCN -
DB-ID BICD2_000009 See all 2 reported entries
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) 0.00464 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BICD2 NM_001003800.1 -?/. - c.269A>G r.(?) p.(Lys90Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.