Variant #0000518143 (NC_000003.11:g.14183277A>G, TMEM43(NM_024334.2):c.1185A>G)

Chromosome 3
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.14183277A>G
DNA change (hg38) g.14141777A>G
Published as TMEM43(NM_024334.2):c.1185A>G (p.P395=)
ISCN -
DB-ID TMEM43_000139
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
XPC NM_004628.4 -?/. - c.*4164T>C r.(=) p.(=) -
TMEM43 NM_024334.2 -?/. - c.1185A>G r.(?) p.(Pro395=) -