Variant #0000701998 (NC_000001.10:g.1167659A>G, B3GALT6(NM_080605.3):c.1A>G)

Individual ID 00318134
Chromosome 1
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1167659A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID B3GALT6_000028 See all 5 reported entries
Variant remarks -
Reference PubMed: Nakajima et al., 2013
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Raymond Dalgleish
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Raymond Dalgleish
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predicted     

Type/DNA     
B3GALT6 NM_080605.3 +?/+? 1 c.1A>G r.(?) p.0? initiating methionine substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000319316 DNA SEQ;SEQ-NG - - B3GALT6 2 Raymond Dalgleish