Variant #0000999714 (NC_000012.11:g.117013942G>T, NM_001085481.1:c.195G>T (MAP1LC3B2))

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.117013942G>T
DNA change (hg38) -
Published as MAP1LC3B2(NM_001085481.3):c.195G>T (p.K65N)
ISCN -
DB-ID MAP1LC3B2_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP1LC3B2 NM_001085481.1 ?/. - c.195G>T r.(?) p.(Lys65Asn)


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