Variant #0000332744 (NC_000009.11:g.111705107A>C, NM_017832.3:c.*3141A>C (FAM206A))

Chromosome 9
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.111705107A>C
DNA change (hg38) g.108942827A>C
Published as CTNNAL1(NM_003798.2):c.2147T>G (p.(Met716Arg))
ISCN -
DB-ID CTNNAL1_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) 0.00278 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNAL1 NM_003798.2 ?/. - c.2147T>G r.(?) p.(Met716Arg)
FAM206A NM_017832.3 ?/. - c.*3141A>C r.(=) p.(=)


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