Variant #0000527209 (NC_000006.11:g.132030176A>G, NM_001145659.1:c.1982T>C (CTAGE9))

Chromosome 6
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.132030176A>G
DNA change (hg38) g.131709036A>G
Published as CTAGE9(NM_001145659.1):c.1982T>C (p.M661T)
ISCN -
DB-ID CTAGE9_000002
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
CTAGE9 NM_001145659.1 -?/. - c.1982T>C r.(?) p.(Met661Thr)
ENPP3 NM_005021.3 -?/. - c.1413-9636A>G r.(=) p.(=)
OR2A4 NM_030908.1 -?/. - c.-7635T>C r.(?) p.(=)


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