Variant #0000321418 (NC_000010.10:g.3178724G>C, NM_014889.3:c.*1499C>G (PITRM1))

Chromosome 10
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.3178724G>C
DNA change (hg38) g.3136532G>C
Published as PFKP(NM_001242339.1):c.2284G>C (p.(Val762Leu))
ISCN -
DB-ID PFKP_000002
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) 0.00122 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFKP NM_002627.4 ?/. - c.2308G>C r.(?) p.(Val770Leu)
PITRM1 NM_014889.3 ?/. - c.*1499C>G r.(=) p.(=)


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