Variant #0000507313 (NC_000001.10:g.36557324_36557328del, NM_017825.2:c.414_418del (ADPRHL2))

Chromosome 1
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.36557324_36557328del
DNA change (hg38) g.36091723_36091727del
Published as ADPRS(NM_017825.3):c.414_418delTGCCC (p.A139Gfs*4)
ISCN -
DB-ID ADPRHL2_000004 See all 3 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL8A2 NM_005202.2 ?/. - c.*5844_*5848del r.(=) p.(=)
TEKT2 NM_014466.2 ?/. - c.*3537_*3541del r.(=) p.(=)
ADPRHL2 NM_017825.2 ?/. - c.414_418del r.(?) p.(Ala139GlyfsTer4)


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