Variant #0000530332 (NC_000007.13:g.107188719G>T, NC_000007.13(NM_006348.3):c.440+4C>A (COG5))

Chromosome 7
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.107188719G>T
DNA change (hg38) g.107548274G>T
Published as COG5(NM_001161520.2):c.347+4C>A
ISCN -
DB-ID DUS4L_000010
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) 0.27037 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 2019-07-18 18:22:55 +02:00 (CEST)
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.*72912G>T r.(=) p.(=)
COG5 NM_006348.3 -/. - c.440+4C>A r.spl? p.?
HBP1 NM_012257.3 -/. - c.*346843G>T r.(=) p.(=)
DUS4L NM_181581.2 -/. - c.-16046G>T r.(?) p.(=)


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