Variant #0000567738 (NC_000019.9:g.45912218A>G, NM_012099.1:c.992A>G (CD3EAP))

Chromosome 19
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.45912218A>G
DNA change (hg38) g.45408960A>G
Published as CD3EAP(NM_012099.1):c.992A>G (p.(Lys331Arg))
ISCN -
DB-ID CD3EAP_000003
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) 2.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC1 NM_001983.3 -?/. - c.*715T>C r.(=) p.(=)
PPP1R13L NM_006663.3 -?/. - c.-3983T>C r.(?) p.(=)
FOSB NM_006732.2 -?/. - c.-59627A>G r.(?) p.(=)
CD3EAP NM_012099.1 -?/. - c.992A>G r.(?) p.(Lys331Arg)


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