Variant #0000610371 (NC_000006.11:g.44121559T>C, NM_018426.1:c.2089T>C (TMEM63B))

Chromosome 6
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.44121559T>C
DNA change (hg38) g.44153822T>C
Published as TMEM63B(NM_018426.1):c.2089T>C (p.(Phe697Leu))
ISCN -
DB-ID TMEM63B_000002 See all 2 reported entries
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-08-07 11:58:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPN11 NM_007058.3 ?/. - c.-5027T>C r.(?) p.(=)
TMEM63B NM_018426.1 ?/. - c.2089T>C r.(?) p.(Phe697Leu)
MRPL14 NM_032111.2 ?/. - c.-26497A>G r.(?) p.(=)


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