Variant #0000316328 (NC_000018.9:g.44560732C>G, NC_000018.9(NM_031303.2):c.-94-18519C>G (KATNAL2))

Chromosome 18
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44560732C>G
DNA change (hg38) g.47034361C>G
Published as TCEB3B(NM_016427.2):c.904G>C (p.D302H)
ISCN -
DB-ID KATNAL2_000006
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) 0.00407 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 2018-01-15 20:58:59 +01:00 (CET)
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     
TCEB3CL NM_001100817.1 -/. - c.-10434G>C r.(?) p.(=)
TCEB3B NM_016427.2 -/. - c.904G>C r.(?) p.(Asp302His)
KATNAL2 NM_031303.2 -/. - c.-94-18519C>G r.(=) p.(=)
TCEB3C NM_145653.3 -/. - c.-4519G>C r.(?) p.(=)


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