Variant #0000534179 (NC_000008.10:g.145154021G>T, NM_030974.3:c.1010C>A (SHARPIN))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.145154021G>T
DNA change (hg38) g.144099118G>T
Published as SHARPIN(NM_030974.4):c.1010C>A (p.P337H)
ISCN -
DB-ID CYC1_000002
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) Retrieve
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     
CYC1 NM_001916.3 ?/. - c.*1782G>T r.(=) p.(=)
SHARPIN NM_030974.3 ?/. - c.1010C>A r.(?) p.(Pro337His)


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