Variant #0000564918 (NC_000018.9:g.44549397G>C, NC_000018.9(NM_031303.2):c.-95+22511G>C (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.44549397G>C
DNA change (hg38) -
Published as ELOA3C(NM_001354366.1):c.902C>G (p.S301C)
ISCN -
DB-ID KATNAL2_000008
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 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.902C>G r.(?) p.(Ser301Cys)
TCEB3B NM_016427.2 -/. - c.*9977C>G r.(=) p.(=)
KATNAL2 NM_031303.2 -/. - c.-95+22511G>C r.(=) p.(=)
TCEB3C NM_145653.3 -/. - c.*5176C>G r.(=) p.(=)


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