Variant #0000252430 (NC_000006.11:g.45390617A>G, NM_001024630.3:c.346A>G (RUNX2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45390617A>G
DNA change (hg38) g.45422880A>G
Published as RUNX2(NM_001024630.4):c.346A>G (p.T116A)
ISCN -
DB-ID RUNX2_000006
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
RUNX2 NM_001024630.3 +?/. - c.346A>G r.(?) p.(Thr116Ala)
SUPT3H NM_181356.2 +?/. - c.-45265T>C r.(?) p.(=)


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