Variant #0000333377 (NC_000023.10:g.19533142C>A, NM_000284.3:c.*155371C>A (PDHA1))

Chromosome X
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.19533142C>A
DNA change (hg38) g.19515024C>A
Published as MAP3K15(NM_001001671.3):c.238G>T (p.(Glu80Ter))
ISCN -
DB-ID MAP3K15_000046
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) Retrieve
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDHA1 NM_000284.3 ?/. - c.*155371C>A r.(=) p.(=)
MAP3K15 NM_001001671.3 ?/. - c.238G>T r.(?) p.(Glu80Ter)


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