Variant #0000316587 (NC_000011.9:g.2190951C>T, NM_199292.2:c.334G>A (TH))

Chromosome 11
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.2190951C>T
DNA change (hg38) g.2169721C>T
Published as TH(NM_199292.2):c.334G>A (p.V112M), TH(NM_199292.3):c.334G>A (p.V112M)
ISCN -
DB-ID TH_000027 See all 4 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) 0.42844 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.241G>A r.(?) p.(Val81Met)
TH NM_199292.2 -/. - c.334G>A r.(?) p.(Val112Met)


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