Variant #0000860363 (NC_000006.11:g.45405790T>A, NC_000006.11(NM_001024630.3):c.685+2T>A (RUNX2))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45405790T>A
DNA change (hg38) -
Published as RUNX2(NM_001024630.3):c.685+2T>A (p.?)
ISCN -
DB-ID SUPT3H_000013
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.685+2T>A r.spl? p.?
SUPT3H NM_181356.2 +/. - c.-60438A>T r.(?) p.(=)


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