Variant #0000311915 (NC_000008.10:g.119964052G>C, NM_006438.3:c.-115469G>C (COLEC10))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119964052G>C
DNA change (hg38) g.118951813G>C
Published as TNFRSF11B(NM_002546.4):c.9C>G (p.N3K)
ISCN -
DB-ID TNFRSF11B_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) 0.52057 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF11B NM_002546.3 -/. - c.9C>G r.(?) p.(Asn3Lys)
COLEC10 NM_006438.3 -/. - c.-115469G>C r.(?) p.(=)


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