Variant #0000517138 (NC_000002.11:g.96942978C>G, NM_014014.4:c.5933G>C (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.96942978C>G
DNA change (hg38) g.96277240C>G
Published as SNRNP200(NM_014014.4):c.5933G>C (p.G1978A)
ISCN -
DB-ID CIAO1_000004
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) 0.00682 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 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     
CIAO1 NM_004804.2 -?/. - c.*5889C>G r.(=) p.(=)
SNRNP200 NM_014014.4 -?/. - c.5933G>C r.(?) p.(Gly1978Ala)


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