Variant #0000524321 (NC_000005.9:g.138160248G>C, NM_001903.2:c.618G>C (CTNNA1))

Chromosome 5
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.138160248G>C
DNA change (hg38) g.138824559G>C
Published as CTNNA1(NM_001290307.2):c.618G>C (p.Q206H), CTNNA1(NM_001290307.3):c.618G>C (p.Q206H), CTNNA1(NM_001323982.2):c.618G>C (p.Q206H), CTNNA1(NM_001903....)
ISCN -
DB-ID CTNNA1_000019 See all 5 reported entries
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) 0.0047 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA1 NM_001903.2 ?/. - c.618G>C r.(?) p.(Gln206His)
LRRTM2 NM_015564.2 ?/. - c.*48451C>G r.(=) p.(=)


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