Variant #0000611516 (NC_000008.10:g.145150101T>G, NM_030974.3:c.*3603A>C (SHARPIN))

Chromosome 8
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.145150101T>G
DNA change (hg38) g.144095198T>G
Published as -
ISCN -
DB-ID CYC1_000003
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) 0.89698 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-24 19:00:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CYC1 NM_001916.3 -/. - c.99T>G r.(?) p.(Arg33=)
SHARPIN NM_030974.3 -/. - c.*3603A>C r.(=) p.(=)


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