Variant #0000890700 (NC_000012.11:g.56845153_56845156del, NM_012064.3:c.705_708del (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.56845153_56845156del
DNA change (hg38) -
Published as MIP(NM_012064.4):c.705_708delTGTC (p.V236Sfs*22)
ISCN -
DB-ID MIP_000015 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TIMELESS NM_003920.3 ?/. - c.-2119_-2116del r.(?) p.(=)
MIP NM_012064.3 ?/. - c.705_708del r.(?) p.(Val236Serfs*22)


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