Variant #0000559122 (NC_000016.9:g.75579362G>A, NM_001077416.2:c.629C>T (TMEM231))

Chromosome 16
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.75579362G>A
DNA change (hg38) g.75545464G>A
Published as TMEM231(NM_001077416.2):c.629C>T (p.A210V)
ISCN -
DB-ID TMEM231_000013 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) 0.00056 View details
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 2024-10-04 09:30:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM231 NM_001077416.2 ?/. - c.629C>T r.(?) p.(Ala210Val)
TMEM231 NM_001077418.2 ?/. - c.470C>T r.(?) p.(Ala157Val)


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