Variant #0001041352 (NC_000016.9:g.75574019C>G, NM_001077416.2:c.983G>C (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.75574019C>G
DNA change (hg38) -
Published as TMEM231(NM_001077418.3):c.824G>C (p.(Ser275Thr))
ISCN -
DB-ID TMEM231_000060
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.983G>C r.(?) p.(Ser328Thr)
TMEM231 NM_001077418.2 ?/. - c.824G>C r.(?) p.(Ser275Thr)
CHST5 NM_024533.4 ?/. - c.-6346G>C r.(?) p.(=)


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