Variant #0000322316 (NC_000011.9:g.65810948C>T, NM_006842.2:c.-8908C>T (SF3B2))

Chromosome 11
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.65810948C>T
DNA change (hg38) g.66043477C>T
Published as GAL3ST3(NM_033036.2):c.326G>A (p.(Arg109His))
ISCN -
DB-ID GAL3ST3_000001
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) 5.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SF3B2 NM_006842.2 -?/. - c.-8908C>T r.(?) p.(=)
GAL3ST3 NM_033036.2 -?/. - c.326G>A r.(?) p.(Arg109His)
CATSPER1 NM_053054.3 -?/. - c.-17098G>A r.(?) p.(=)


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