Variant #0000555501 (NC_000015.9:g.75648381A>G, NC_000015.9(NM_006715.3):c.2997-8T>C (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.75648381A>G
DNA change (hg38) g.75356040A>G
Published as MAN2C1(NM_006715.4):c.2997-8T>C
ISCN -
DB-ID MAN2C1_000003
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) 0.0003 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAN2C1 NM_006715.3 -?/. - c.2997-8T>C r.(=) p.(=)
NEIL1 NM_024608.3 -?/. - c.*1006A>G r.(=) p.(=)


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