Variant #0000544953 (NC_000011.9:g.64825877G>T, NM_005468.2:c.117C>A (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.64825877G>T
DNA change (hg38) g.65058405G>T
Published as NAALADL1(NM_005468.3):c.117C>A (p.D39E)
ISCN -
DB-ID NAALADL1_000007
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) 0.00017 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAALADL1 NM_005468.2 ?/. - c.117C>A r.(?) p.(Asp39Glu)
SAC3D1 NM_013299.3 ?/. - c.*13678G>T r.(=) p.(=)


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