Variant #0000561262 (NC_000017.10:g.38244626G>A, NM_001190918.1:c.855G>A (THRA))

Chromosome 17
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.38244626G>A
DNA change (hg38) g.40088373G>A
Published as THRA(NM_003250.6):c.855G>A (p.E285=)
ISCN -
DB-ID THRA_000006
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) 0.00015 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.855G>A r.(?) p.(Glu285=)
NR1D1 NM_021724.3 -/. - c.*4710C>T r.(=) p.(=)


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