Variant #0000800847 (NC_000002.11:g.9630536G>A, NM_003183.4:c.2245C>T (ADAM17))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.9630536G>A
DNA change (hg38) -
Published as ADAM17(NM_003183.6):c.2245C>T (p.P749S)
ISCN -
DB-ID ADAM17_000029
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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     
IAH1 NM_001039613.1 -?/. - c.*2078G>A r.(=) p.(=)
ADAM17 NM_003183.4 -?/. - c.2245C>T r.(?) p.(Pro749Ser)


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