Variant #0000528991 (NC_000006.11:g.46669588G>A, NM_001168357.1:c.*2709C>T (PLA2G7))

Chromosome 6
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.46669588G>A
DNA change (hg38) g.46701851G>A
Published as TDRD6(NM_001010870.2):c.6262-7G>A (p.(=))
ISCN -
DB-ID PLA2G7_000005
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) Retrieve
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     
TDRD6 NM_001010870.2 -?/. - c.6262-7G>A r.(=) p.(=)
PLA2G7 NM_001168357.1 -?/. - c.*2709C>T r.(=) p.(=)


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