Variant #0000862609 (NC_000011.9:g.62393883G>A, NM_012200.3:c.-4464C>T (B3GAT3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62393883G>A
DNA change (hg38) -
Published as GANAB(NM_001278192.1):c.2272C>T (p.(His758Tyr)), GANAB(NM_198335.4):c.2614C>T (p.H872Y)
ISCN -
DB-ID GANAB_000002 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) 0.00256 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +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     
B3GAT3 NM_012200.3 -/. - c.-4464C>T r.(?) p.(=)
GANAB NM_198335.3 -/. - c.2614C>T r.(?) p.(His872Tyr)


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