Variant #0000614355 (NC_000012.11:g.6439831A>G, NM_001065.3:c.672T>C (TNFRSF1A))

Chromosome 12
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.6439831A>G
DNA change (hg38) g.6330665A>G
Published as TNFRSF1A(NM_001065.3):c.672T>C (p.L224=)
ISCN -
DB-ID PLEKHG6_000016
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) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-02 12:22:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF1A NM_001065.3 -?/. - c.672T>C r.(?) p.(Leu224=)
PLEKHG6 NM_018173.3 -?/. - c.*2520A>G r.(=) p.(=)


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