Variant #0000851366 (NC_000007.13:g.106938662G>A, NM_006348.3:c.1331C>T (COG5))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.106938662G>A
DNA change (hg38) -
Published as COG5(NM_001161520.1):c.1331C>T (p.T444I)
ISCN -
DB-ID DUS4L_000035
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR22 NM_005295.2 -?/. - c.-173186G>A r.(?) p.(=)
COG5 NM_006348.3 -?/. - c.1331C>T r.(?) p.(Thr444Ile)
HBP1 NM_012257.3 -?/. - c.*96786G>A r.(=) p.(=)
DUS4L NM_181581.2 -?/. - c.-266103G>A r.(?) p.(=)


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