Variant #0000338955 (NC_000002.11:g.96943473T>C, NC_000002.11(NM_014014.4):c.5755-20A>G (SNRNP200))

Chromosome 2
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.96943473T>C
DNA change (hg38) g.96277735T>C
Published as SNRNP200(NM_014014.5):c.5755-20A>G
ISCN -
DB-ID SNRNP200_000011 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) 0.36963 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 2018-01-15 20:58:59 +01:00 (CET)
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     
CIAO1 NM_004804.2 -/. - c.*6384T>C r.(=) p.(=)
SNRNP200 NM_014014.4 -/. - c.5755-20A>G r.(=) p.(=)


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