Variant #0000000029 (NC_000017.10:g.42990647T>C, GFAP(NM_002055.4):c.770A>G)

Individual ID 00000029
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.42990647T>C
Reference Howard KL1, Hall DA, Moon M, Agarwal P, Newman E, Brenner M.(2008)
DB-ID GFAP_000038
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     
GFAP NM_002055.4 ./. 4 c.770A>G r.(?) p.(Tyr257Cys) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000029 ? ? GFAP 1 Y Yang