Variant #0000322299 (NC_000011.9:g.64811763G>T, NM_005468.2:c.*980C>A (NAALADL1))

Chromosome 11
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.64811763G>T
DNA change (hg38) g.65044291G>T
Published as SAC3D1(NM_013299.3):c.641G>T (p.(Arg214Leu))
ISCN -
DB-ID SAC3D1_000002
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) 0.00011 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARL2 NM_001667.3 -?/. - c.*22436G>T r.(=) p.(=)
NAALADL1 NM_005468.2 -?/. - c.*980C>A r.(=) p.(=)
SAC3D1 NM_013299.3 -?/. - c.641G>T r.(?) p.(Arg214Leu)
SNX15 NM_013306.4 -?/. - c.*4499G>T r.(=) p.(=)


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