Variant #0001046066 (NC_000006.11:g.45480010C>T, NM_001024630.3:c.887C>T (RUNX2))

Chromosome 6
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.45480010C>T
DNA change (hg38) -
Published as RUNX2(NM_001024630.4):c.887C>T (p.P296L)
ISCN -
DB-ID SUPT3H_000036
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) 0.00017 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 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RUNX2 NM_001024630.3 -?/. - c.887C>T r.(?) p.(Pro296Leu)
SUPT3H NM_181356.2 -?/. - c.-134658G>A r.(?) p.(=)


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