Variant #0001002300 (NC_000016.9:g.3338567C>G, NM_033208.3:c.*10398G>C (TIGD7))

Chromosome 16
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.3338567C>G
DNA change (hg38) -
Published as ZNF263(NM_005741.4):c.883C>G (p.(Pro295Ala))
ISCN -
DB-ID TIGD7_000001
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) 0.00052 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 2024-08-28 13:16:32 +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     
ZNF263 NM_005741.4 ?/. - c.883C>G r.(?) p.(Pro295Ala)
TIGD7 NM_033208.3 ?/. - c.*10398G>C r.(=) p.(=)


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