Variant #0000728245 (NC_000023.10:g.100356092G>A, CENPI(NM_006733.2):c.33G>A)

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.100356092G>A
DNA change (hg38) -
Published as CENPI(NM_006733.3):c.33G>A (p.Q11=)
ISCN -
DB-ID TMEM35_000018
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) 0.00022 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.33G>A r.(?) p.(Gln11=)
TMEM35 NM_021637.2 -?/. - c.*6147G>A r.(=) p.(=)