Variant #0000322975 (NC_000012.11:g.58159173C>G, NM_138396.5:c.*6493C>G (MARCH9))

Chromosome 12
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.58159173C>G
DNA change (hg38) g.57765390C>G
Published as CYP27B1(NM_000785.3):c.496G>C (p.(Val166Leu))
ISCN -
DB-ID CYP27B1_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) 0.00993 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP27B1 NM_000785.3 -?/. - c.496G>C r.(?) p.(Val166Leu) -
METTL1 NM_005371.5 -?/. - c.*3606G>C r.(=) p.(=) -
MARCH9 NM_138396.5 -?/. - c.*6493C>G r.(=) p.(=) -


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