Variant #0000559121 (NC_000016.9:g.75579250G>A, NM_001077416.2:c.741C>T (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.75579250G>A
DNA change (hg38) g.75545352G>A
Published as TMEM231(NM_001077418.3):c.582C>T (p.N194=)
ISCN -
DB-ID TMEM231_000024
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) 0.00015 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 2024-04-07 09:33:52 +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.741C>T r.(?) p.(Asn247=)
TMEM231 NM_001077418.2 -?/. - c.582C>T r.(?) p.(Asn194=)


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