Variant #0000325905 (NC_000018.9:g.44554703A>C, NC_000018.9(NM_031303.2):c.-94-24548A>C (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.44554703A>C
DNA change (hg38) g.47028332A>C
Published as TCEB3C(NM_145653.3):c.1511T>G (p.(Val504Gly))
ISCN -
DB-ID KATNAL2_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.-4405T>G r.(?) p.(=)
TCEB3B NM_016427.2 -?/. - c.*4671T>G r.(=) p.(=)
KATNAL2 NM_031303.2 -?/. - c.-94-24548A>C r.(=) p.(=)
TCEB3C NM_145653.3 -?/. - c.1511T>G r.(?) p.(Val504Gly)


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