Variant #0001051006 (NC_000002.11:g.202357871C>T, NM_001168221.1:c.3193G>A (ALS2CR11))

Chromosome 2
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.202357871C>T
DNA change (hg38) -
Published as C2CD6(NM_001168221.2):c.3193G>A (p.(Glu1065Lys))
ISCN -
DB-ID STRADB_000005
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) 0.00037 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALS2CR11 NM_001168221.1 ?/. - c.3193G>A r.(?) p.(Glu1065Lys)
STRADB NM_018571.5 ?/. - c.*12973C>T r.(=) p.(=)


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