Variant #0000313332 (NC_000009.11:g.108536246G>C, NM_018112.2:c.761G>C (TMEM38B))

Chromosome 9
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.108536246G>C
DNA change (hg38) g.105773965G>C
Published as TMEM38B(NM_018112.1):c.761G>C (p.(Cys254Ser)), TMEM38B(NM_018112.3):c.761G>C (p.C254S)
ISCN -
DB-ID TMEM38B_000104 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) 0.0135 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM38B NM_018112.2 -/. - c.761G>C r.(?) p.(Cys254Ser)


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