Variant #0000800852 (NC_000002.11:g.96944340C>T, NM_014014.4:c.5433G>A (SNRNP200))

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.96944340C>T
DNA change (hg38) -
Published as SNRNP200(NM_014014.4):c.5433G>A (p.A1811=)
ISCN -
DB-ID CIAO1_000011
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) 0.00013 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CIAO1 NM_004804.2 -?/. - c.*7251C>T r.(=) p.(=)
SNRNP200 NM_014014.4 -?/. - c.5433G>A r.(?) p.(Ala1811=)


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