Variant #0000933692 (NC_000009.11:g.108456984A>C, NM_018112.2:c.43A>C (TMEM38B))

Chromosome 9
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.108456984A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID TMEM38B_000112
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs138722007
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00023 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-09-27 11:08:01 +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     
TMEM38B NM_018112.2 ?/. - c.43A>C r.(?) p.(Thr15Pro)


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