Variant #0000546622 (NC_000012.11:g.11214568T>C, NM_006250.3:c.-177752A>G (PRH1))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11214568T>C
DNA change (hg38) g.11061969T>C
Published as TAS2R46(NM_176887.2):c.326A>G (p.K109R)
ISCN -
DB-ID PRH1_000016
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAS2R30 NM_001097643.1 ?/. - c.*71316A>G r.(=) p.(=)
PRH2 NM_001110213.1 ?/. - c.*129762T>C r.(=) p.(=)
PRH1 NM_006250.3 ?/. - c.-177752A>G r.(?) p.(=)
TAS2R13 NM_023920.2 ?/. - c.-152671A>G r.(?) p.(=)
TAS2R14 NM_023922.1 ?/. - c.-122762A>G r.(?) p.(=)
TAS2R43 NM_176884.2 ?/. - c.*29331A>G r.(=) p.(=)
TAS2R31 NM_176885.2 ?/. - c.-30634A>G r.(?) p.(=)
TAS2R46 NM_176887.2 ?/. - c.326A>G r.(?) p.(Lys109Arg)
TAS2R19 NM_176888.1 ?/. - c.-39398A>G r.(?) p.(=)
TAS2R20 NM_176889.2 ?/. - c.-64094A>G r.(?) p.(=)
TAS2R50 NM_176890.2 ?/. - c.-75109A>G r.(?) p.(=)


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