Variant #0000924521 (NC_000006.11:g.45390590_45390591del, NM_001024630.3:c.319_320del (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.45390590_45390591del
DNA change (hg38) -
Published as RUNX2(NM_001369405.1):c.277_278delGC (p.A93Rfs*53)
ISCN -
DB-ID SUPT3H_000021
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +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.319_320del r.(?) p.(Ala107Argfs*53)
SUPT3H NM_181356.2 +/. - c.-45238_-45237del r.(?) p.(=)


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