Variant #0000562707 (NC_000017.10:g.62081070C>T, NM_001191029.1:c.*1735C>T (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.62081070C>T
DNA change (hg38) g.64003710C>T
Published as ICAM2(NM_001099786.1):c.583G>A (p.D195N)
ISCN -
DB-ID C17orf72_000002
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 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     
ICAM2 NM_000873.3 ?/. - c.583G>A r.(?) p.(Asp195Asn)
C17orf72 NM_001191029.1 ?/. - c.*1735C>T r.(=) p.(=)


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