Variant #0000658240 (NC_000017.10:g.71199854A>G, NM_018714.2:c.2304A>G (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.71199854A>G
DNA change (hg38) g.73203715A>G
Published as COG1(NM_018714.2):c.2304A>G (p.T768=)
ISCN -
DB-ID COG1_000024
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) 0.00121 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-14 10:57:53 +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.2304A>G r.(?) p.(Thr768=)
FAM104A NM_032837.2 -?/. - c.*5814T>C r.(=) p.(=)


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