Variant #0000655695 (NC_000007.13:g.107204349G>A, NM_006348.3:c.86C>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.107204349G>A
DNA change (hg38) g.107563904G>A
Published as COG5(NM_001161520.2):c.-8C>T
ISCN -
DB-ID DUS4L_000028
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) 2.0E-5 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 2020-03-23 16:13:27 +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     
GPR22 NM_005295.2 -?/. - c.*88542G>A r.(=) p.(=)
COG5 NM_006348.3 -?/. - c.86C>T r.(?) p.(Pro29Leu)
HBP1 NM_012257.3 -?/. - c.*362473G>A r.(=) p.(=)
DUS4L NM_181581.2 -?/. - c.-416G>A r.(?) p.(=)


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