Variant #0000890081 (NC_000011.9:g.65824765C>T, NM_006842.2:c.696C>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.65824765C>T
DNA change (hg38) -
Published as SF3B2(NM_006842.3):c.696C>T (p.P232=)
ISCN -
DB-ID CATSPER1_000008
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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SF3B2 NM_006842.2 -?/. - c.696C>T r.(?) p.(Pro232=)
GAL3ST3 NM_033036.2 -?/. - c.-8396G>A r.(?) p.(=)
CATSPER1 NM_053054.3 -?/. - c.-30915G>A r.(?) p.(=)


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