Variant #0001026481 (NC_000015.9:g.65370260C>G, NM_001101362.2:c.1107C>G (KBTBD13))

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.65370260C>G
DNA change (hg38) -
Published as KBTBD13(NM_001101362.2):c.1107C>G (p.I369M), KBTBD13(NM_001101362.3):c.1107C>G (p.I369M)
ISCN -
DB-ID KBTBD13_000022 See all 3 reported entries
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) 2.0E-5 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 2025-02-07 18:57:27 +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     
KBTBD13 NM_001101362.2 ?/. - c.1107C>G r.(?) p.(Ile369Met)


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