Variant #0000538483 (NC_000009.11:g.77502394_77502395dup, NC_000009.11(NM_017662.4):c.33+345_33+346dup (TRPM6))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.77502394_77502395dup
DNA change (hg38) g.74887478_74887479dup
Published as TRPM6(NM_017662.5):c.33+345_33+346dupTG
ISCN -
DB-ID TRPM6_000053
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPM6 NM_017662.4 -/. - c.33+345_33+346dup r.(=) p.(=)


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