Variant #0000308679 (NC_000002.11:g.96950323C>T, NM_014014.4:c.4165G>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.96950323C>T
DNA change (hg38) g.96284585C>T
Published as SNRNP200(NM_014014.4):c.4165G>A (p.V1389I), SNRNP200(NM_014014.5):c.4165G>A (p.V1389I)
ISCN -
DB-ID SNRNP200_000003 See all 4 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) 0.00548 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNRNP200 NM_014014.4 -?/. - c.4165G>A r.(?) p.(Val1389Ile)


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