Variant #0000514860 (NC_000002.11:g.220435375G>A, OBSL1(NM_001173408.1):c.580C>T)

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.220435375G>A
DNA change (hg38) g.219570653G>A
Published as OBSL1(NM_015311.3):c.580C>T (p.L194=)
ISCN -
DB-ID OBSL1_000018 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) 0.42815 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OBSL1 NM_001173408.1 -/. - c.580C>T r.(?) p.(Leu194=)
INHA NM_002191.3 -/. - c.-1722G>A r.(?) p.(=)