Variant #0000925697 (NC_000012.11:g.6927665T>C, NM_000616.4:c.1235T>C (CD4))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6927665T>C
DNA change (hg38) -
Published as CD4(NM_000616.5):c.1235T>C (p.I412T)
ISCN -
DB-ID CD4_000006
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) 0.0024 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 2023-04-16 21:50:28 +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     
CD4 NM_000616.4 -/. - c.1235T>C r.(?) p.(Ile412Thr)
GPR162 NM_019858.1 -/. - c.-3833T>C r.(?) p.(=)


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