Variant #0000250671 (NC_000010.10:g.69281701A>T, NM_013266.2:c.478T>A (CTNNA3))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.69281701A>T
DNA change (hg38) g.67521943A>T
Published as CTNNA3(NM_013266.3):c.478T>A (p.S160T), CTNNA3(NM_013266.4):c.478T>A (p.S160T, p.(Ser160Thr))
ISCN -
DB-ID CTNNA3_000086 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) 0.02337 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNNA3 NM_013266.2 -/. - c.478T>A r.(?) p.(Ser160Thr)
LRRTM3 NM_178011.3 -/. - c.*424147A>T r.(=) p.(=)


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