Variant #0000558892 (NC_000016.9:g.69377396T>G, NM_032382.4:c.-3941A>C (COG8))

Chromosome 16
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.69377396T>G
DNA change (hg38) g.69343493T>G
Published as TMED6(NM_144676.3):c.637A>C (p.(Ile213Leu))
ISCN -
DB-ID COG8_000013
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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     
NIP7 NM_016101.4 -?/. - c.*1841T>G r.(=) p.(=)
PDF NM_022341.1 -?/. - c.-12923A>C r.(?) p.(=)
COG8 NM_032382.4 -?/. - c.-3941A>C r.(?) p.(=)
TMED6 NM_144676.3 -?/. - c.637A>C r.(?) p.(Ile213Leu)


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