Variant #0000612487 (NC_000010.10:g.51580586C>A, NM_001145260.1:c.220C>A (NCOA4))

Chromosome 10
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.51580586C>A
DNA change (hg38) g.46015236G>T
Published as NCOA4(NM_001145260.1):c.220C>A (p.R74S)
ISCN -
DB-ID MSMB_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
NCOA4 NM_001145260.1 ?/. - c.220C>A r.(?) p.(Arg74Ser)
MSMB NM_002443.3 ?/. - c.*18186C>A r.(=) p.(=)
NCOA4 NM_005437.3 ?/. - c.172C>A r.(?) p.(Arg58Ser)
TIMM23 NM_006327.3 ?/. - c.*11918G>T r.(=) p.(=)


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