Variant #0000017973 (NC_000001.10:g.89847539T>C, NC_000001.10(NM_198460.2):c.1152+6T>C (GBP6))

Chromosome 1
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.89847539T>C
DNA change (hg38) g.89381980T>C
Published as -
ISCN -
DB-ID GBP6_000001
Variant remarks variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 1
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00183 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-05-06 10:12:12 +02:00 (CEST)
Date last edited 2014-10-05 12:34:31 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GBP6 NM_198460.2 ?/? ?i c.1152+6T>C r.(spl?) p.(=)


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