Variant #0000613770 (NC_000011.9:g.85365174A>G, NM_032273.3:c.154A>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.85365174A>G
DNA change (hg38) g.85654130A>G
Published as TMEM126A(NM_032273.3):c.154A>G (p.S52G), TMEM126A(NM_032273.4):c.154A>G (p.S52G)
ISCN -
DB-ID TMEM126A_000007 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) 0.00285 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 2019-12-04 15:24:38 +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.*9681T>C r.(=) p.(=)
TMEM126A NM_032273.3 -?/. - c.154A>G r.(?) p.(Ser52Gly)


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