Variant #0000968518 (NC_000016.9:g.75589749C>T, NM_001077416.2:c.421G>A (TMEM231))

Chromosome 16
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.75589749C>T
DNA change (hg38) -
Published as TMEM231(NM_001077416.2):c.421G>A (p.A141T)
ISCN -
DB-ID TMEM231_000018
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM231 NM_001077416.2 -?/. - c.421G>A r.(?) p.(Ala141Thr)
TMEM231 NM_001077418.2 -?/. - c.262G>A r.(?) p.(Ala88Thr)


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