Variant #0000569956 (NC_000020.10:g.49551779_49551780insA, NM_015339.2:c.-4598_-4597insT (ADNP))

Chromosome 20
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.49551779_49551780insA
DNA change (hg38) g.50935242_50935243insA
Published as DPM1(NM_003859.1):c.679-7_679-6insT (p.(=)), DPM1(NM_003859.2):c.679-7_679-6insT
ISCN -
DB-ID DPM1_000006 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPM1 NM_003859.1 -/. - c.679-7_679-6insT r.(=) p.(=)
ADNP NM_015339.2 -/. - c.-4598_-4597insT r.(?) p.(=)


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