Variant #0000893176 (NC_000016.9:g.75579762C>T, NM_001077416.2:c.559G>A (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.75579762C>T
DNA change (hg38) -
Published as TMEM231(NM_001077416.2):c.559G>A (p.G187S)
ISCN -
DB-ID TMEM231_000052
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +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.559G>A r.(?) p.(Gly187Ser)
TMEM231 NM_001077418.2 ?/. - c.400G>A r.(?) p.(Gly134Ser)


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