Variant #0000999848 (NC_000012.11:g.133303841A>C, NM_015114.1:c.2804T>G (ANKLE2))

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.133303841A>C
DNA change (hg38) -
Published as ANKLE2(NM_015114.1):c.2804T>G (p.(Leu935Arg))
ISCN -
DB-ID ANKLE2_000023
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) 0.00013 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKLE2 NM_015114.1 -?/. - c.2804T>G r.(?) p.(Leu935Arg)
PGAM5 NM_138575.3 -?/. - c.*8445A>C r.(=) p.(=)


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