Variant #0000000831 (NC_000017.10:g.3385088T>C, ASPA(NM_000049.2):c.428T>C)

Individual ID 00000831
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.3385088T>C
Reference Kobayashi K1, Tsujino S, Ezoe T, Hamaguchi H, Nihei K, Sakuragawa N.(1998)
DB-ID ASPA_000016
Frequency -
Average frequency (gnomAD v.2.1.1) 0 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     
ASPA NM_000049.2 ./. 2 c.428T>C r.(?) p.(Ile143Thr) 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     
0000000831 ? ? ASPA 1 Y Yang