Variant #0000248237 (NC_000016.9:g.75579233A>T, NC_000016.9(NM_001077416.2):c.741+17T>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.75579233A>T
DNA change (hg38) g.75545335A>T
Published as TMEM231(NM_001077416.2):c.741+17T>A
ISCN -
DB-ID TMEM231_000010 See all 2 reported entries
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) 0.23981 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-07-30 13:25:17 +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.741+17T>A r.(=) p.(=)
TMEM231 NM_001077418.2 -/. - c.582+17T>A r.(=) p.(=)


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