Variant #0000974374 (NC_000002.11:g.160721355T>A, NM_014880.4:c.-66646A>T (CD302))

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.160721355T>A
DNA change (hg38) -
Published as LY75-CD302(NM_001198759.1):c.2194A>T (p.(Thr732Ser))
ISCN -
DB-ID CD302_000001
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) 5.0E-5 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 2024-04-19 20:20:39 +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     
LY75-CD302 NM_001198759.1 ?/. - c.2194A>T r.(?) p.(Thr732Ser)
LY75 NM_002349.3 ?/. - c.2194A>T r.(?) p.(Thr732Ser)
CD302 NM_014880.4 ?/. - c.-66646A>T r.(?) p.(=)


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