Variant #0000269863 (NC_000012.11:g.6559330T>C, NM_014231.3:c.*14306A>G (VAMP1))

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.6559330T>C
DNA change (hg38) g.6450164T>C
Published as CD27(NM_001242.4):c.269-9T>C
ISCN -
DB-ID CD27_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) 0.0064 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 2018-01-15 20:58:59 +01:00 (CET)
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     
CD27 NM_001242.4 -/. - c.269-9T>C r.(=) p.(=)
VAMP1 NM_014231.3 -/. - c.*14306A>G r.(=) p.(=)
TAPBPL NM_018009.4 -/. - c.-2085T>C r.(?) p.(=)
CD27-AS1 NR_015382.1 -/. - n.1177+177A>G r.(?) -


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