Variant #0000565128 (NC_000018.9:g.55335796_55335802dup, NC_000018.9(NM_005603.4):c.2098-21_2098-15dup (ATP8B1))

Chromosome 18
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.55335796_55335802dup
DNA change (hg38) g.57668564_57668570dup
Published as ATP8B1(NM_005603.6):c.2098-21_2098-15dupTTTTTTT
ISCN -
DB-ID ATP8B1_000031
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP8B1 NM_005603.4 -/. - c.2098-21_2098-15dup r.(=) p.(=)


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