Variant #0001035469 (NC_000006.11:g.130467191T>C, NM_001007102.2:c.*6293T>C (L3MBTL3))

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.130467191T>C
DNA change (hg38) -
Published as SAMD3(NM_001017373.4):c.1159A>G (p.(Lys387Glu))
ISCN -
DB-ID L3MBTL3_000004
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) 0.00023 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
L3MBTL3 NM_001007102.2 ?/. - c.*6293T>C r.(=) p.(=)
SAMD3 NM_001258275.1 ?/. - c.1159A>G r.(?) p.(Lys387Glu)


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