Variant #0000266881 (NC_000013.10:g.40229957T>A, NM_001145079.1:c.94T>A (COG6))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.40229957T>A
DNA change (hg38) g.39655820T>A
Published as COG6(NM_001145079.2):c.94T>A (p.C32S), COG6(NM_020751.3):c.94T>A (p.C32S)
ISCN -
DB-ID COG6_000003 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.45845 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG6 NM_001145079.1 -/. - c.94T>A r.(?) p.(Cys32Ser)


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