Variant #0000311844 (NC_000011.9:g.2188676C>T, NM_199292.2:c.777G>A (TH))

Chromosome 11
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.2188676C>T
DNA change (hg38) g.2167446C>T
Published as TH(NM_199292.2):c.777G>A (p.E259=), TH(NM_199292.3):c.777G>A (p.E259=)
ISCN -
DB-ID TH_000018 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) 0.00556 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TH NM_000360.3 -?/. - c.684G>A r.(?) p.(Glu228=)
TH NM_199292.2 -?/. - c.777G>A r.(?) p.(Glu259=)


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