Variant #0000314231 (NC_000006.11:g.45296618T>C, NC_000006.11(NM_001024630.3):c.58+97T>C (RUNX2))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45296618T>C
DNA change (hg38) g.45328881T>C
Published as SUPT3H(NM_181356.3):c.-51-5914A>G
ISCN -
DB-ID SUPT3H_000001
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.58+97T>C r.(=) p.(=)
SUPT3H NM_181356.2 ?/. - c.-51-5914A>G r.(=) p.(=)


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