Variant #0000322679 (NC_000012.11:g.11214387C>A, NM_006250.3:c.-177571G>T (PRH1))

Chromosome 12
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.11214387C>A
DNA change (hg38) g.11061788C>A
Published as TAS2R46(NM_176887.2):c.507G>T (p.(Arg169Ser))
ISCN -
DB-ID TAS2R46_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAS2R30 NM_001097643.1 -?/. - c.*71497G>T r.(=) p.(=)
PRH2 NM_001110213.1 -?/. - c.*129581C>A r.(=) p.(=)
PRH1 NM_006250.3 -?/. - c.-177571G>T r.(?) p.(=)
TAS2R13 NM_023920.2 -?/. - c.-152490G>T r.(?) p.(=)
TAS2R14 NM_023922.1 -?/. - c.-122581G>T r.(?) p.(=)
TAS2R43 NM_176884.2 -?/. - c.*29512G>T r.(=) p.(=)
TAS2R31 NM_176885.2 -?/. - c.-30453G>T r.(?) p.(=)
TAS2R46 NM_176887.2 -?/. - c.507G>T r.(?) p.(Arg169Ser)
TAS2R19 NM_176888.1 -?/. - c.-39217G>T r.(?) p.(=)
TAS2R20 NM_176889.2 -?/. - c.-63913G>T r.(?) p.(=)
TAS2R50 NM_176890.2 -?/. - c.-74928G>T r.(?) p.(=)


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