Variant #0000722785 (NC_000010.10:g.21309059T>C, NM_006393.2:c.-122925A>G (NEBL))

Chromosome 10
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.21309059T>C
DNA change (hg38) -
Published as NEBL(NM_213569.2):c.236A>G (p.E79G)
ISCN -
DB-ID C10orf113_000066
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf113 NM_001010896.2 ?/. - c.*105693A>G r.(=) p.(=)
NEBL NM_006393.2 ?/. - c.-122925A>G r.(?) p.(=)


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