Variant #0000992963 (NC_000002.11:g.55461320T>C, NM_002453.2:c.*2464A>G (MTIF2))

Chromosome 2
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.55461320T>C
DNA change (hg38) -
Published as RPS27A(NM_002954.5):c.169T>C (p.(Ser57Pro))
ISCN -
DB-ID RPS27A_000001 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) 0.001 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 2024-08-28 13:16:32 +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.169T>C r.(?) p.(Ser57Pro)
MTIF2 NM_002453.2 ?/. - c.*2464A>G r.(=) p.(=)
CLHC1 NM_152385.2 ?/. - c.-2217A>G r.(?) p.(=)


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