Variant #0000616498 (NC_000017.10:g.38240080C>T, NC_000017.10(NM_001190918.1):c.223-8C>T (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.38240080C>T
DNA change (hg38) g.40083827C>T
Published as THRA(NM_001190918.1):c.223-8C>T (p.(=)), THRA(NM_003250.6):c.223-8C>T
ISCN -
DB-ID THRA_000011 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) 0.00458 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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.223-8C>T r.(=) p.(=)


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