Variant #0000535028 (NC_000008.10:g.59409504_59409505insA, NM_000780.3:c.566_567insT (CYP7A1))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.59409504_59409505insA
DNA change (hg38) g.58496945_58496946insA
Published as CYP7A1(NM_000780.4):c.566_567insT (p.R190Qfs*18)
ISCN -
DB-ID CYP7A1_000048
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP7A1 NM_000780.3 +/. - c.566_567insT r.(?) p.(Arg190GlnfsTer18) -


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