Variant #0000923794 (NC_000002.11:g.96919855T>C, NC_000002.11(NM_017849.3):c.410-2A>G (TMEM127))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.96919855T>C
DNA change (hg38) -
Published as TMEM127(NM_001193304.3):c.410-2A>G, TMEM127(NM_017849.4):c.410-2A>G
ISCN -
DB-ID TMEM127_000028 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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.410-2A>G r.spl? p.?


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