Variant #0000677275 (NC_000004.11:g.39462502A>G, NM_194451.1:c.138A>G (LIAS))

Chromosome 4
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.39462502A>G
DNA change (hg38) -
Published as LIAS(NM_006859.3):c.138A>G (p.Q46=)
ISCN -
DB-ID LIAS_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL9 NM_000661.4 -?/. - c.-1993T>C r.(?) p.(=)
LIAS NM_194451.1 -?/. - c.138A>G r.(?) p.(Gln46=)


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