Variant #0000677925 (NC_000007.13:g.107204433A>G, NM_006348.3:c.2T>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.107204433A>G
DNA change (hg38) -
Published as COG5(NM_001161520.1):c.2T>C (p.M1?)
ISCN -
DB-ID DUS4L_000030
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) 5.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR22 NM_005295.2 ?/. - c.*88626A>G r.(=) p.(=)
COG5 NM_006348.3 ?/. - c.2T>C r.(?) p.(Met1?)
HBP1 NM_012257.3 ?/. - c.*362557A>G r.(=) p.(=)
DUS4L NM_181581.2 ?/. - c.-332A>G r.(?) p.(=)


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