Variant #0000892278 (NC_000015.9:g.75649215G>A, NM_006715.3:c.2576C>T (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.75649215G>A
DNA change (hg38) -
Published as MAN2C1(NM_001256494.1):c.2627C>T (p.S876L)
ISCN -
DB-ID NEIL1_000004
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +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.2576C>T r.(?) p.(Ser859Leu)
NEIL1 NM_024608.3 ?/. - c.*1840G>A r.(=) p.(=)


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