Variant #0000548820 (NC_000012.11:g.58157930C>T, NM_138396.5:c.*5250C>T (MARCH9))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.58157930C>T
DNA change (hg38) g.57764147C>T
Published as CYP27B1(NM_000785.3):c.1166G>A (p.R389H), CYP27B1(NM_000785.4):c.1166G>A (p.R389H)
ISCN -
DB-ID CYP27B1_000002 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) 0.0001 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP27B1 NM_000785.3 +/. - c.1166G>A r.(?) p.(Arg389His) -
METTL1 NM_005371.5 +/. - c.*4849G>A r.(=) p.(=) -
MARCH9 NM_138396.5 +/. - c.*5250C>T r.(=) p.(=) -


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