Variant #0001038819 (NC_000011.9:g.837964A>C, NM_004357.4:c.638A>C (CD151))

Chromosome 11
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.837964A>C
DNA change (hg38) -
Published as CD151(NM_004357.5):c.638A>C (p.(Glu213Ala))
ISCN -
DB-ID CD151_000029
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPAN4 NM_001025234.1 ?/. - c.-6340A>C r.(?) p.(=)
CD151 NM_004357.4 ?/. - c.638A>C r.(?) p.(Glu213Ala)
POLR2L NM_021128.4 ?/. - c.*2408T>G r.(=) p.(=)


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