Variant #0001015888 (NC_000021.8:g.36164605A>G, NM_001754.4:c.1270T>C (RUNX1))

Chromosome 21
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.36164605A>G
DNA change (hg38) -
Published as RUNX1(NM_001001890.2):c.1189T>C (p.(Ser397Pro)), RUNX1(NM_001754.4):c.1270T>C (p.S424P), RUNX1(NM_001754.5):c.1270T>C (p.S424P)
ISCN -
DB-ID RUNX1_000015 See all 3 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RUNX1 NM_001754.4 ?/. - c.1270T>C r.(?) p.(Ser424Pro)


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