Variant #0000864778 (NC_000016.9:g.3573221T>C, NM_015041.2:c.777T>C (CLUAP1))

Chromosome 16
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.3573221T>C
DNA change (hg38) -
Published as CLUAP1(NM_015041.3):c.777T>C (p.Y259=)
ISCN -
DB-ID NLRC3_000006
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLUAP1 NM_015041.2 -?/. - c.777T>C r.(?) p.(Tyr259=)
NLRC3 NM_178844.2 -?/. - c.*18604A>G r.(=) p.(=)


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