Variant #0000681313 (NC_000019.9:g.1491330T>C, NM_138393.1:c.62T>C (REEP6))

Chromosome 19
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.1491330T>C
DNA change (hg38) -
Published as REEP6(NM_001329556.2):c.62T>C (p.V21A)
ISCN -
DB-ID PCSK4_000010
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCSK4 NM_017573.3 -?/. - c.-985A>G r.(?) p.(=)
REEP6 NM_138393.1 -?/. - c.62T>C r.(?) p.(Val21Ala)


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