Variant #0001045332 (NC_000013.10:g.74289642A>C, NM_007249.4:c.890T>G (KLF12))

Chromosome 13
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.74289642A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID KLF12_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs891600489
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-10 13:11:01 +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     
KLF12 NM_007249.4 ?/. - c.890T>G r.(?) p.(Ile297Ser)


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