Variant #0000944867 (NC_000014.8:g.81528523C>T, NM_000369.2:c.202C>T (TSHR))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.81528523C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSHR_000026 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs142063461
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00055 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-15 17:43:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSHR NM_000369.2 +?/. - c.202C>T r.(?) p.(Pro68Ser)


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