Variant #0000562927 (NC_000017.10:g.71193525G>C, NM_018714.2:c.903G>C (COG1))

Chromosome 17
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.71193525G>C
DNA change (hg38) g.73197386G>C
Published as COG1(NM_018714.2):c.903G>C (p.(Gln301His)), COG1(NM_018714.3):c.903G>C (p.Q301H)
ISCN -
DB-ID COG1_000018 See all 3 reported entries
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) 0.00563 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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG1 NM_018714.2 -?/. - c.903G>C r.(?) p.(Gln301His)
FAM104A NM_032837.2 -?/. - c.*12143C>G r.(=) p.(=)


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