Variant #0000689998 (NC_000007.13:g.40173948del, NM_138701.3:c.221del (MPLKIP))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40173948del
DNA change (hg38) -
Published as MPLKIP(NM_138701.3):c.221delC (p.P74Rfs*79)
ISCN -
DB-ID C7orf10_000008
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 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C7orf10 NM_001193313.1 +?/. - c.-651del r.(?) p.(=)
MPLKIP NM_138701.3 +?/. - c.221del r.(?) p.(Pro74ArgfsTer79)


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