Variant #0000561265 (NC_000017.10:g.38250363G>A, NM_001190918.1:c.*728G>A (THRA))

Chromosome 17
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.38250363G>A
DNA change (hg38) g.40094110G>A
Published as NR1D1(NM_021724.4):c.1447C>T (p.(Arg483Cys))
ISCN -
DB-ID THRA_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) 0 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
THRA NM_001190918.1 -?/. - c.*728G>A r.(=) p.(=)
NR1D1 NM_021724.3 -?/. - c.1447C>T r.(?) p.(Arg483Cys)


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