Variant #0000528979 (NC_000006.11:g.45390514_45390531del, NM_001024630.3:c.243_260del (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.45390514_45390531del
DNA change (hg38) g.45422777_45422794del
Published as RUNX2(NM_001015051.3):c.216_233del (p.(Ala84_Ala89del)), RUNX2(NM_001024630.4):c.243_260delGGCGGCTGCGGCGGCGGC (p.A84_A89del)
ISCN -
DB-ID RUNX2_000004 See all 2 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
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.243_260del r.(?) p.(Ala84_Ala89del)
SUPT3H NM_181356.2 -?/. - c.-45152_-45135del r.(?) p.(=)


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