Variant #0000314555 (NC_000016.9:g.75573837C>T, NM_001077416.2:c.*55G>A (TMEM231))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.75573837C>T
DNA change (hg38) g.75539939C>T
Published as TMEM231(NR_074083.2):n.1172G>A
ISCN -
DB-ID TMEM231_000005
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*55G>A r.(=) p.(=)
TMEM231 NM_001077418.2 -/. - c.*55G>A r.(=) p.(=)
CHST5 NM_024533.4 -/. - c.-6164G>A r.(?) p.(=)


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