Variant #0000914369 (NC_000015.9:g.75648650C>T, NM_006715.3:c.2878G>A (MAN2C1))

Chromosome 15
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.75648650C>T
DNA change (hg38) -
Published as MAN2C1(NM_001256494.1):c.2929G>A (p.(Val977Ile))
ISCN -
DB-ID NEIL1_000007
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) 0.04407 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAN2C1 NM_006715.3 -?/. - c.2878G>A r.(?) p.(Val960Ile)
NEIL1 NM_024608.3 -?/. - c.*1275C>T r.(=) p.(=)


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