Variant #0000945925 (NC_000015.9:g.75649173T>C, NM_006715.3:c.2618A>G (MAN2C1))

Chromosome 15
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.75649173T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID MAN2C1_000013
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs776736788
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-21 15:14:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAN2C1 NM_006715.3 ?/. - c.2618A>G r.(?) p.(Tyr873Cys)


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