Variant #0000296340 (NC_000010.10:g.51568378T>G, NM_001145260.1:c.22T>G (NCOA4))

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.51568378T>G
DNA change (hg38) g.46027444A>C
Published as NCOA4(NM_001145260.2):c.22T>G (p.F8V)
ISCN -
DB-ID NCOA4_000005
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) 0.44597 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.22T>G r.(?) p.(Phe8Val)
MSMB NM_002443.3 -/. - c.*5978T>G r.(=) p.(=)
NCOA4 NM_005437.3 -/. - c.-4129T>G r.(?) p.(=)
TIMM23 NM_006327.3 -/. - c.*24126A>C r.(=) p.(=)


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