Variant #0000805883 (NC_000012.11:g.58158240G>C, NM_138396.5:c.*5560G>C (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.58158240G>C
DNA change (hg38) -
Published as CYP27B1(NM_000785.3):c.1057C>G (p.P353A)
ISCN -
DB-ID CYP27B1_000010
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) 0.00041 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 2021-09-17 14:40:49 +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.1057C>G r.(?) p.(Pro353Ala) -
METTL1 NM_005371.5 -?/. - c.*4539C>G r.(=) p.(=) -
MARCH9 NM_138396.5 -?/. - c.*5560G>C r.(=) p.(=) -


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