Variant #0000984595 (NC_000023.10:g.19373632C>G, NC_000023.10(NM_000284.3):c.759+10C>G (PDHA1))

Chromosome X
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.19373632C>G
DNA change (hg38) -
Published as PDHA1(NM_000284.4):c.759+10C>G, PDHA1(NM_001173454.1):c.873+10C>G
ISCN -
DB-ID MAP3K15_000086 See all 2 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) 0.00012 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 2024-04-19 20:27:30 +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     
PDHA1 NM_000284.3 -?/. - c.759+10C>G r.(=) p.(=)
MAP3K15 NM_001001671.3 -?/. - c.*5235G>C r.(=) p.(=)


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