Variant #0000316586 (NC_000011.9:g.2190961C>G, NM_199292.2:c.324G>C (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.2190961C>G
DNA change (hg38) g.2169731C>G
Published as TH(NM_199292.2):c.324G>C (p.E108D)
ISCN -
DB-ID TH_000028
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) Retrieve
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 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.231G>C r.(?) p.(Glu77Asp)
TH NM_199292.2 -?/. - c.324G>C r.(?) p.(Glu108Asp)


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