Variant #0000853209 (NC_000011.9:g.838115A>G, NC_000011.9(NM_004357.4):c.703-18A>G (CD151))

Chromosome 11
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.838115A>G
DNA change (hg38) -
Published as CD151(NM_004357.5):c.703-18A>G
ISCN -
DB-ID CD151_000018
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) 0.00139 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +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     
TSPAN4 NM_001025234.1 -?/. - c.-6189A>G r.(?) p.(=)
CD151 NM_004357.4 -?/. - c.703-18A>G r.(=) p.(=)
POLR2L NM_021128.4 -?/. - c.*2257T>C r.(=) p.(=)


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