Variant #0000572533 (NC_000023.10:g.100356235A>G, CENPI(NM_006733.2):c.176A>G)

Chromosome X
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.100356235A>G
DNA change (hg38) g.101101246A>G
Published as CENPI(NM_006733.3):c.176A>G (p.D59G)
ISCN -
DB-ID TMEM35_000017
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
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CENPI NM_006733.2 -?/. - c.176A>G r.(?) p.(Asp59Gly)
TMEM35 NM_021637.2 -?/. - c.*6290A>G r.(=) p.(=)