Variant #0000515022 (NC_000002.11:g.231042380G>A, NM_080424.2:c.1464C>T (SP110))

Chromosome 2
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.231042380G>A
DNA change (hg38) g.230177664G>A
Published as SP110(NM_004509.4):c.1464C>T (p.C488=), SP110(NM_080424.2):c.1464C>T (p.C488=)
ISCN -
DB-ID SP110_000015 See all 2 reported entries
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) 0.00502 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SP110 NM_080424.2 -?/. - c.1464C>T r.(?) p.(Cys488=)


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