Variant #0001004139 (NC_000018.9:g.44603829C>T, NM_031303.2:c.992C>T (KATNAL2))

Chromosome 18
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.44603829C>T
DNA change (hg38) -
Published as KATNAL2(NM_031303.2):c.992C>T (p.(Pro331Leu))
ISCN -
DB-ID KATNAL2_000030
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) 1.0E-5 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 2024-08-28 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     
TCEB3CL NM_001100817.1 ?/. - c.-53531G>A r.(?) p.(=)
TCEB3B NM_016427.2 ?/. - c.-42194G>A r.(?) p.(=)
KATNAL2 NM_031303.2 ?/. - c.992C>T r.(?) p.(Pro331Leu)
TCEB3C NM_145653.3 ?/. - c.-47616G>A r.(?) p.(=)


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