Variant #0000610604 (NC_000007.13:g.107204416_107204417insGCC, NM_006348.3:c.18_19insGGC (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.107204416_107204417insGCC
DNA change (hg38) g.107563971_107563972insGCC
Published as COG5(NM_001161520.1):c.18_19insGGC (p.(Gly6dup))
ISCN -
DB-ID DUS4L_000025
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*88609_*88610insGCC r.(=) p.(=)
COG5 NM_006348.3 -?/. - c.18_19insGGC r.(?) p.(Gly6dup)
HBP1 NM_012257.3 -?/. - c.*362540_*362541insGCC r.(=) p.(=)
DUS4L NM_181581.2 -?/. - c.-349_-348insGCC r.(?) p.(=)


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