Variant #0000548710 (NC_000012.11:g.56845066dup, NM_012064.3:c.790dup (MIP))

Chromosome 12
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.56845066dup
DNA change (hg38) g.56451282dup
Published as MIP(NM_012064.4):c.790dupT (p.*264Lfs*7)
ISCN -
DB-ID MIP_000003
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 16:30:37 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TIMELESS NM_003920.3 ?/. - c.-2034dup r.(?) p.(=)
MIP NM_012064.3 ?/. - c.790dup r.(?) p.(Ter264LeuextTer6)


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