Variant #0000992722 (NC_000002.11:g.241439903G>A, NM_017844.2:c.1667C>T (ANKMY1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.241439903G>A
DNA change (hg38) -
Published as ANKMY1(NM_001282771.1):c.2606C>T (p.(Thr869Ile))
ISCN -
DB-ID ANKMY1_000002
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 2024-08-28 13:07:21 +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     
DUSP28 NM_001033575.1 ?/. - c.-60199G>A r.(?) p.(=)
ANKMY1 NM_017844.2 ?/. - c.1667C>T r.(?) p.(Thr556Ile)


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