Variant #0000546000 (NC_000011.9:g.85367449G>A, NM_032273.3:c.492G>A (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.85367449G>A
DNA change (hg38) g.85656405G>A
Published as TMEM126A(NM_032273.4):c.492G>A (p.L164=)
ISCN -
DB-ID CREBZF_000003
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) 0.00014 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CREBZF NM_001039618.2 -?/. - c.*7406C>T r.(=) p.(=)
TMEM126A NM_032273.3 -?/. - c.492G>A r.(?) p.(Leu164=)


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