Variant #0000890751 (NC_000012.11:g.6560055T>C, NM_014231.3:c.*13581A>G (VAMP1))

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.6560055T>C
DNA change (hg38) -
Published as CD27(NM_001242.4):c.539-6T>C
ISCN -
DB-ID CD27_000010
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) 0.00021 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD27 NM_001242.4 -?/. - c.539-6T>C r.(=) p.(=)
VAMP1 NM_014231.3 -?/. - c.*13581A>G r.(=) p.(=)
TAPBPL NM_018009.4 -?/. - c.-1360T>C r.(?) p.(=)
CD27-AS1 NR_015382.1 -?/. - n.629A>G r.(?) -


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