Variant #0000999252 (NC_000011.9:g.64812150T>C, NM_005468.2:c.*593A>G (NAALADL1))

Chromosome 11
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.64812150T>C
DNA change (hg38) -
Published as SAC3D1(NM_013299.3):c.1028T>C (p.(Met343Thr))
ISCN -
DB-ID ARL2_000003
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
Date created 2024-08-28 13:16:32 +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     
ARL2 NM_001667.3 ?/. - c.*22823T>C r.(=) p.(=)
NAALADL1 NM_005468.2 ?/. - c.*593A>G r.(=) p.(=)
SAC3D1 NM_013299.3 ?/. - c.1028T>C r.(?) p.(Met343Thr)
SNX15 NM_013306.4 ?/. - c.*4886T>C r.(=) p.(=)


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