Variant #0001037149 (NC_000009.11:g.117087401A>G, NM_000607.2:c.509A>G (ORM1))

Chromosome 9
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.117087401A>G
DNA change (hg38) -
Published as ORM1(NM_000607.4):c.509A>G (p.(Lys170Arg))
ISCN -
DB-ID ORM1_000001
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) 0.00739 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ORM1 NM_000607.2 -?/. - c.509A>G r.(?) p.(Lys170Arg)
ORM2 NM_000608.2 -?/. - c.-4784A>G r.(?) p.(=)


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