Variant #0000316669 (NC_000011.9:g.85365116T>G, NM_032273.3:c.96T>G (TMEM126A))

Chromosome 11
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.85365116T>G
DNA change (hg38) g.85654072T>G
Published as TMEM126A(NM_032273.3):c.96T>G (p.L32=)
ISCN -
DB-ID TMEM126A_000006
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) 0.00189 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 10:59:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CREBZF NM_001039618.2 -?/. - c.*9739A>C r.(=) p.(=)
TMEM126A NM_032273.3 -?/. - c.96T>G r.(?) p.(Leu32=)


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