Variant #0001033420 (NC_000002.11:g.55460017C>T, NM_002453.2:c.*3767G>A (MTIF2))

Chromosome 2
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.55460017C>T
DNA change (hg38) -
Published as RPS27A(NM_002954.6):c.48+9C>T
ISCN -
DB-ID MTIF2_000004
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) 0.0466 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
RPS27A NM_001135592.2 -?/. - c.48+9C>T r.(=) p.(=)
MTIF2 NM_002453.2 -?/. - c.*3767G>A r.(=) p.(=)
CLHC1 NM_152385.2 -?/. - c.-914G>A r.(?) p.(=)


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