Variant #0000564922 (NC_000018.9:g.44561007C>T, NC_000018.9(NM_031303.2):c.-94-18244C>T (KATNAL2))

Chromosome 18
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.44561007C>T
DNA change (hg38) g.47034636C>T
Published as TCEB3B(NM_016427.2):c.629G>A (p.(Gly210Asp))
ISCN -
DB-ID KATNAL2_000012
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) 0.00075 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 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     
TCEB3CL NM_001100817.1 -?/. - c.-10709G>A r.(?) p.(=)
TCEB3B NM_016427.2 -?/. - c.629G>A r.(?) p.(Gly210Asp)
KATNAL2 NM_031303.2 -?/. - c.-94-18244C>T r.(=) p.(=)
TCEB3C NM_145653.3 -?/. - c.-4794G>A r.(?) p.(=)


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