Variant #0000325572 (NC_000017.10:g.71193106G>A, NM_018714.2:c.628G>A (COG1))

Chromosome 17
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.71193106G>A
DNA change (hg38) g.73196967G>A
Published as COG1(NM_018714.2):c.628G>A (p.(Glu210Lys))
ISCN -
DB-ID COG1_000005
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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     
COG1 NM_018714.2 ?/. - c.628G>A r.(?) p.(Glu210Lys)
FAM104A NM_032837.2 ?/. - c.*12562C>T r.(=) p.(=)


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