Variant #0000887540 (NC_000007.13:g.107198453T>G, NM_006348.3:c.295A>C (COG5))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.107198453T>G
DNA change (hg38) -
Published as COG5(NM_001161520.1):c.295A>C (p.(Ile99Leu)), COG5(NM_006348.5):c.202A>C (p.I68L)
ISCN -
DB-ID DUS4L_000012 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 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR22 NM_005295.2 ?/. - c.*82646T>G r.(=) p.(=)
COG5 NM_006348.3 ?/. - c.295A>C r.(?) p.(Ile99Leu)
HBP1 NM_012257.3 ?/. - c.*356577T>G r.(=) p.(=)
DUS4L NM_181581.2 ?/. - c.-6312T>G r.(?) p.(=)


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