Variant #0000950654 (NC_000016.9:g.3580590C>T, NM_015041.2:c.951C>T (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.3580590C>T
DNA change (hg38) -
Published as CLUAP1(NM_001330454.2):c.951C>T (p.D317=)
ISCN -
DB-ID NLRC3_000010
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) 1.0E-5 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 2023-11-27 17:35:39 +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     
CLUAP1 NM_015041.2 -?/. - c.951C>T r.(?) p.(=)
NLRC3 NM_178844.2 -?/. - c.*11235G>A r.(=) p.(=)


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