Variant #0000249103 (NC_000007.13:g.107198405A>T, NC_000007.13(NM_006348.3):c.327+16T>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.107198405A>T
DNA change (hg38) g.107557960A>T
Published as COG5(NM_001161520.2):c.234+16T>A
ISCN -
DB-ID COG5_000004
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) 0.42594 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 2018-01-15 20:58:59 +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.*82598A>T r.(=) p.(=)
COG5 NM_006348.3 -/. - c.327+16T>A r.(=) p.(=)
HBP1 NM_012257.3 -/. - c.*356529A>T r.(=) p.(=)
DUS4L NM_181581.2 -/. - c.-6360A>T r.(?) p.(=)


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