Variant #0000002798 (NC_000015.9:g.68504054G>A, CLN6(NM_017882.2):c.445C>T)

Individual ID 00002798
Chromosome 15
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.68504054G>A
Reference Ray pers comm
DB-ID CLN6_000023 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 6.0E-5 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 ./. 4 c.445C>T r.(?) p.(Arg149Cys) 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     
0000002798 ? ? CLN6 1 Y Yang