Variant #0000999633 (NC_000012.11:g.11286438G>A, NM_006250.3:c.-249622C>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.11286438G>A
DNA change (hg38) -
Published as TAS2R30(NM_001097643.1):c.406C>T (p.(Pro136Ser))
ISCN -
DB-ID PRH1_000043
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAS2R30 NM_001097643.1 -?/. - c.406C>T r.(?) p.(Pro136Ser)
PRH2 NM_001110213.1 -?/. - c.*201632G>A r.(=) p.(=)
PRH1 NM_006250.3 -?/. - c.-249622C>T r.(?) p.(=)
TAS2R13 NM_023920.2 -?/. - c.-224541C>T r.(?) p.(=)
TAS2R14 NM_023922.1 -?/. - c.-194632C>T r.(?) p.(=)
TAS2R43 NM_176884.2 -?/. - c.-41610C>T r.(?) p.(=)
TAS2R31 NM_176885.2 -?/. - c.-102504C>T r.(?) p.(=)
TAS2R46 NM_176887.2 -?/. - c.-71545C>T r.(?) p.(=)
TAS2R19 NM_176888.1 -?/. - c.-111268C>T r.(?) p.(=)
TAS2R20 NM_176889.2 -?/. - c.-135964C>T r.(?) p.(=)
TAS2R50 NM_176890.2 -?/. - c.-146979C>T r.(?) p.(=)


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