Variant #0000859931 (NC_000005.9:g.38933303A>G, NM_003999.2:c.2697A>G (OSMR))

Chromosome 5
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.38933303A>G
DNA change (hg38) -
Published as OSMR(NM_003999.2):c.2697A>G (p.K899=), OSMR(NM_003999.3):c.2697A>G (p.K899=)
ISCN -
DB-ID OSMR_000012 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) 0.00047 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OSMR NM_003999.2 -?/. - c.2697A>G r.(?) p.(Lys899=)
RICTOR NM_152756.3 -?/. - c.*9103T>C r.(=) p.(=)


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