Variant #0001046071 (NC_000006.11:g.54002927C>A, NM_001281747.2:c.2060C>A (MLIP))

Chromosome 6
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.54002927C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MLIP_000016
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLIP NM_001281747.2 ?/. - c.2060C>A r.(?) p.(Thr687Asn)
MLIP NM_138569.2 ?/. - c.613-10927C>A r.(=) p.(=)


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