Variant #0000001456 (NC_000017.10:g.42427661T>C, GRN(NM_002087.2):c.415T>C)

Individual ID 00001456
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.42427661T>C
Reference Piaceri I1, Pradella S1, Cupidi C2, Nannucci S1, Polito C3, Bagnoli S1, Tedde A1, Smirne N2, Anfossi M2, Gallo M2, Bernardi L2, Colao R2, Maletta R2, Bruni AC2, Sorbi S1, Nacmias B1.(2014)
DB-ID GRN_000010 See all 4 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00018 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
GRN NM_002087.2 ./. 5 c.415T>C r.(?) p.(Cys139Arg) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001456 ? ? GRN 1 Y Yang