Variant #0001003576 (NC_000017.10:g.62082604A>G, NM_001191029.1:c.*3269A>G (C17orf72))

Chromosome 17
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.62082604A>G
DNA change (hg38) -
Published as ICAM2(NM_001099789.1):c.191T>C (p.(Leu64Pro))
ISCN -
DB-ID C17orf72_000007
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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
ICAM2 NM_000873.3 ?/. - c.191T>C r.(?) p.(Leu64Pro)
C17orf72 NM_001191029.1 ?/. - c.*3269A>G r.(=) p.(=)


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