Variant #0000968517 (NC_000016.9:g.75573823T>A, NM_001077416.2:c.*69A>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.75573823T>A
DNA change (hg38) -
Published as TMEM231(NM_001077418.1):c.*69A>T (p.(=))
ISCN -
DB-ID TMEM231_000058
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*69A>T r.(=) p.(=)
TMEM231 NM_001077418.2 -?/. - c.*69A>T r.(=) p.(=)
CHST5 NM_024533.4 -?/. - c.-6150A>T r.(?) p.(=)


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