Variant #0000997726 (NC_000009.11:g.140082356T>C, NM_001128228.2:c.*4208A>G (TPRN))

Chromosome 9
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.140082356T>C
DNA change (hg38) -
Published as ANAPC2(NM_013366.3):c.317A>G (p.(Gln106Arg))
ISCN -
DB-ID ANAPC2_000011
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) 0.00071 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     
TPRN NM_001128228.2 -?/. - c.*4208A>G r.(=) p.(=)
SSNA1 NM_003731.2 -?/. - c.-823T>C r.(?) p.(=)
ANAPC2 NM_013366.3 -?/. - c.317A>G r.(?) p.(Gln106Arg)


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