Variant #0000992376 (NC_000002.11:g.202483711G>A, NM_001044385.2:c.*5267C>T (TMEM237))

Chromosome 2
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.202483711G>A
DNA change (hg38) -
Published as ALS2CR11(NM_001168221.1):c.143C>T (p.(Ala48Val))
ISCN -
DB-ID TMEM237_000040
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) 0.00048 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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     
TMEM237 NM_001044385.2 -?/. - c.*5267C>T r.(=) p.(=)
ALS2CR11 NM_001168221.1 -?/. - c.143C>T r.(?) p.(Ala48Val)


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