Variant #0000298090 (NC_000006.11:g.108233929G>A, NM_007214.4:c.564C>T (SEC63))

Chromosome 6
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.108233929G>A
DNA change (hg38) g.107912725G>A
Published as SEC63(NM_007214.4):c.564C>T (p.N188=), SEC63(NM_007214.5):c.564C>T (p.N188=)
ISCN -
DB-ID SEC63_000006 See all 3 reported entries
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) 0.8589 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEC63 NM_007214.4 -/. - c.564C>T r.(?) p.(Asn188=)


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