Variant #0000608153 (NC_000002.11:g.9630413T>C, NM_003183.4:c.2368A>G (ADAM17))

Chromosome 2
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.9630413T>C
DNA change (hg38) g.9490284T>C
Published as ADAM17(NM_003183.6):c.2368A>G (p.K790E)
ISCN -
DB-ID ADAM17_000021
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IAH1 NM_001039613.1 ?/. - c.*1955T>C r.(=) p.(=)
ADAM17 NM_003183.4 ?/. - c.2368A>G r.(?) p.(Lys790Glu)


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