Variant #0000309210 (NC_000011.9:g.85366671G>A, NM_032273.3:c.314G>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.85366671G>A
DNA change (hg38) g.85655627G>A
Published as TMEM126A(NM_032273.3):c.314G>A (p.R105Q), TMEM126A(NM_032273.4):c.314G>A (p.R105Q)
ISCN -
DB-ID TMEM126A_000011 See all 2 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) 0.00308 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 2018-01-15 20:58:59 +01:00 (CET)
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.*8184C>T r.(=) p.(=)
TMEM126A NM_032273.3 -?/. - c.314G>A r.(?) p.(Arg105Gln)


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