Variant #0000613868 (NC_000012.11:g.11244252_11244257del, NM_006250.3:c.-207441_-207436del (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.11244252_11244257del
DNA change (hg38) g.11091653_11091658del
Published as TAS2R43(NM_176884.2):c.572_577del (p.(Thr191_Leu193delinsIle))
ISCN -
DB-ID PRH1_000027
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 2019-12-04 15:24:38 +01:00 (CET)
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.*41627_*41632del r.(=) p.(=)
PRH2 NM_001110213.1 ?/. - c.*159446_*159451del r.(=) p.(=)
PRH1 NM_006250.3 ?/. - c.-207441_-207436del r.(?) p.(=)
TAS2R13 NM_023920.2 ?/. - c.-182360_-182355del r.(?) p.(=)
TAS2R14 NM_023922.1 ?/. - c.-152451_-152446del r.(?) p.(=)
TAS2R43 NM_176884.2 ?/. - c.572_577del r.(?) p.(Thr191_Leu193delinsIle)
TAS2R31 NM_176885.2 ?/. - c.-60323_-60318del r.(?) p.(=)
TAS2R46 NM_176887.2 ?/. - c.-29364_-29359del r.(?) p.(=)
TAS2R19 NM_176888.1 ?/. - c.-69087_-69082del r.(?) p.(=)
TAS2R20 NM_176889.2 ?/. - c.-93783_-93778del r.(?) p.(=)
TAS2R50 NM_176890.2 ?/. - c.-104798_-104793del r.(?) p.(=)


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