Variant #0000503084 (NC_000001.10:g.150525555G>C, NM_019032.4:c.260G>C (ADAMTSL4))

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.150525555G>C
DNA change (hg38) g.150553079G>C
Published as ADAMTSL4(NM_001288608.1):c.260G>C (p.R87P), ADAMTSL4(NM_019032.4):c.260G>C (p.(Arg87Pro))
ISCN -
DB-ID ADAMTSL4_000057 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 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTSL4 NM_019032.4 ?/. - c.260G>C r.(?) p.(Arg87Pro)


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