Variant #0001047199 (NC_000002.11:g.96920434G>A, NC_000002.11(NM_017849.3):c.409+137C>T (TMEM127))

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.96920434G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TMEM127_000090
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs150996178
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 2025-08-06 17:45:01 +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     
TMEM127 NM_017849.3 -?/. - c.409+137C>T r.(?) p.(?)


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