Variant #0000984890 (NC_000023.10:g.92927498G>C, NM_173698.2:c.-2020G>C (FAM133A))

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.92927498G>C
DNA change (hg38) -
Published as NAP1L3(NM_004538.6):c.806C>G (p.(Thr269Arg))
ISCN -
DB-ID NAP1L3_000013
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) 0.00054 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAP1L3 NM_004538.5 -?/. - c.806C>G r.(?) p.(Thr269Arg)
FAM133A NM_173698.2 -?/. - c.-2020G>C r.(?) p.(=)


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