Variant #0000545048 (NC_000011.9:g.65790365C>G, NM_006842.2:c.-29491C>G (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.65790365C>G
DNA change (hg38) g.66022894C>G
Published as CATSPER1(NM_053054.3):c.1384G>C (p.V462L)
ISCN -
DB-ID CATSPER1_000005
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SF3B2 NM_006842.2 -?/. - c.-29491C>G r.(?) p.(=)
GAL3ST3 NM_033036.2 -?/. - c.*19613G>C r.(=) p.(=)
CATSPER1 NM_053054.3 -?/. - c.1384G>C r.(?) p.(Val462Leu)


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