Variant #0000975660 (NC_000003.11:g.174814870C>T, NM_207015.2:c.334C>T (NAALADL2))

Chromosome 3
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.174814870C>T
DNA change (hg38) -
Published as NAALADL2(NM_207015.3):c.334C>T (p.(Arg112*))
ISCN -
DB-ID NAALADL2_000006
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) 0.0004 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 2024-04-19 20:27:30 +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     
NAALADL2 NM_207015.2 -?/. - c.334C>T r.(?) p.(Arg112*)
NAALADL2-AS3 NR_046390.1 -?/. - n.110+15464G>A r.(?) -


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