Variant #0000690288 (NC_000008.10:g.59409234G>T, NM_000780.3:c.837C>A (CYP7A1))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.59409234G>T
DNA change (hg38) -
Published as CYP7A1(NM_000780.3):c.837C>A (p.H279Q), CYP7A1(NM_000780.4):c.837C>A (p.H279Q)
ISCN -
DB-ID CYP7A1_000042 See all 2 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) 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 2020-09-15 15:50:26 +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.837C>A r.(?) p.(His279Gln) -


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