Variant #0000250052 (NC_000019.9:g.8645786A>C, NM_030957.2:c.3303= (ADAMTS10))

Chromosome 19
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.8645786A>C
DNA change (hg38) g.8580902A>C
Published as ADAMTS10(NM_030957.3):c.3303T>G (p.H1101Q), ADAMTS10(NM_030957.4):c.3303T>G (p.H1101Q)
ISCN -
DB-ID ADAMTS10_000010 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) 0.99988 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO1F NM_012335.3 -/. - c.-3593T>G r.(?) p.(=)
ADAMTS10 NM_030957.2 -/. - c.3303= r.(=) p.(Gln1101=)


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