Variant #0000000749 (NC_000017.10:g.4849202T>A, PFN1(NM_005022.3):c.416A>T)

Individual ID 00000749
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.4849202T>A
Reference Smith BN1, Vance C1, Scotter EL1, Troakes C1, Wong CH1, Topp S1, Maekawa S1, King A1, Mitchell JC1, Lund K1, Al-Chalabi A1, Ticozzi N2, Silani V2, Sapp P3, Brown RH Jr3, Landers JE3, Al-Sarraj S1, Shaw CE4.(2015)
DB-ID PFN1_000005
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
PFN1 NM_005022.3 ./. 3 c.416A>T r.(?) p.(Gln139Leu) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000749 ? ? PFN1 1 Y Yang