Variant #0000000039 (NC_000017.10:g.42990750C>G, GFAP(NM_002055.4):c.667G>C)

Individual ID 00000039
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.42990750C>G
Reference Brockmann K1, Meins M, Taubert A, Trappe R, Grond M, Hanefeld F.(2003)
DB-ID GFAP_000045 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00035 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     
GFAP NM_002055.4 ./. 4 c.667G>C r.(?) p.(Glu223Gln) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000039 ? ? GFAP 1 Y Yang