Variant #0001068956 (NC_000002.11:g.96931002_96931005del, NM_017849.3:c.117_120del (TMEM127))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.96931002_96931005del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TMEM127_000041 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121908816
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 2026-03-05 16:26:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM127 NM_017849.3 +/. - c.117_120del r.(?) p.(Ile41ArgfsTer39)


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