Variant #0000514839 (NC_000002.11:g.220422686C>T, OBSL1(NM_001173408.1):c.*3920G>A)

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.220422686C>T
DNA change (hg38) g.219557964C>T
Published as OBSL1(NM_001173408.1):c.*3920G>A (p.(=)), OBSL1(NM_015311.3):c.3649G>A (p.E1217K)
ISCN -
DB-ID OBSL1_000035 See all 3 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) 0.00509 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OBSL1 NM_001173408.1 -/. - c.*3920G>A r.(=) p.(=)