Variant #0000290596 (NC_000023.10:g.153130950C>T, L1CAM(NM_000425.4):c.2553G>A)

Chromosome X
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.153130950C>T
DNA change (hg38) g.153865495C>T
Published as L1CAM(NM_001278116.1):c.2553G>A (p.T851=)
ISCN -
DB-ID L1CAM_000013
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
L1CAM NM_000425.4 -?/. - c.2553G>A r.(?) p.(Thr851=)