Variant #0001039399 (NC_000012.11:g.58159088C>T, NM_138396.5:c.*6408C>T (MARCH9))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.58159088C>T
DNA change (hg38) -
Published as CYP27B1(NM_000785.4):c.581G>A (p.(Gly194Glu), p.G194E)
ISCN -
DB-ID CYP27B1_000013 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) Retrieve
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     

Haplotype     
CYP27B1 NM_000785.3 ?/. - c.581G>A r.(?) p.(Gly194Glu) -
METTL1 NM_005371.5 ?/. - c.*3691G>A r.(=) p.(=) -
MARCH9 NM_138396.5 ?/. - c.*6408C>T r.(=) p.(=) -


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