Variant #0000249400 (NC_000016.9:g.75589726A>G, NM_001077416.2:c.444T>C (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.75589726A>G
DNA change (hg38) g.75555828A>G
Published as TMEM231(NM_001077416.2):c.444T>C (p.D148=)
ISCN -
DB-ID TMEM231_000017
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.444T>C r.(?) p.(Asp148=)
TMEM231 NM_001077418.2 -?/. - c.285T>C r.(?) p.(Asp95=)


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