Variant #0000316704 (NC_000003.11:g.14183166G>A, TMEM43(NM_024334.2):c.1074G>A)

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.14183166G>A
DNA change (hg38) g.14141666G>A
Published as TMEM43(NM_024334.2):c.1074G>A (p.S358=)
ISCN -
DB-ID TMEM43_000083
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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.*4275C>T r.(=) p.(=) -
TMEM43 NM_024334.2 -?/. - c.1074G>A r.(?) p.(Ser358=) -