Variant #0001052400 (NC_000006.11:g.54002335T>A, NM_001281747.2:c.1468T>A (MLIP))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54002335T>A
DNA change (hg38) -
Published as MLIP(NM_001281747.2):c.1468T>A (p.(Ser490Thr))
ISCN -
DB-ID MLIP_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
MLIP NM_001281747.2 -?/. - c.1468T>A r.(?) p.(Ser490Thr)
MLIP NM_138569.2 -?/. - c.613-11519T>A r.(=) p.(=)


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