Variant #0001054040 (NC_000011.9:g.93462868G>C, NM_033395.1:c.7488G>C (KIAA1731))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.93462868G>C
DNA change (hg38) -
Published as CEP295(NM_033395.2):c.7488G>C (p.(Gln2496His))
ISCN -
DB-ID KIAA1731_000012
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF1D NM_024116.3 ?/. - c.*6459C>G r.(=) p.(=)
KIAA1731 NM_033395.1 ?/. - c.7488G>C r.(?) p.(Gln2496His)


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