Variant #0000658241 (NC_000017.10:g.71202836_71202837del, NC_000017.10(NM_018714.2):c.2620-11_2620-10del (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.71202836_71202837del
DNA change (hg38) g.73206697_73206698del
Published as COG1(NM_018714.2):c.2620-11_2620-10delTT
ISCN -
DB-ID COG1_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) 4.0E-5 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG1 NM_018714.2 -?/. - c.2620-11_2620-10del r.(=) p.(=)
FAM104A NM_032837.2 -?/. - c.*2831_*2832del r.(=) p.(=)


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