Variant #0000528955 (NC_000006.11:g.44108783A>G, NM_018426.1:c.730A>G (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.44108783A>G
DNA change (hg38) g.44141046A>G
Published as TMEM63B(NM_001318792.1):c.730A>G (p.I244V)
ISCN -
DB-ID TMEM63B_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_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 2023-08-07 11:57:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM63B NM_018426.1 ?/. - c.730A>G r.(?) p.(Ile244Val)
MRPL14 NM_032111.2 ?/. - c.-13721T>C r.(?) p.(=)


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