Variant #0000336097 (NC_000023.10:g.153135360T>C, L1CAM(NM_000425.4):c.1021A>G)

Chromosome X
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.153135360T>C
DNA change (hg38) g.153869905T>C
Published as L1CAM(NM_000425.3):c.1021A>G (p.(Ser341Gly))
ISCN -
DB-ID L1CAM_000025
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
L1CAM NM_000425.4 ?/. - c.1021A>G r.(?) p.(Ser341Gly)