Variant #0000002929 (NC_000015.9:g.68521889C>T, CLN6(NM_017882.2):c.34G>A)

Individual ID 00002929
Chromosome 15
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.68521889C>T
Reference Kousi M1, Lehesjoki AE, Mole SE.(2012)
DB-ID CLN6_000047
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00997 View details
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     
CLN6 NM_017882.2 ./. 1 c.34G>A r.(?) p.(Ala12Thr) 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     
0000002929 ? ? CLN6 1 Y Yang