Variant #0000848349 (NC_000001.10:g.159174683T>C, NM_021189.3:c.*3971T>C (CADM3))

Chromosome 1
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.159174683T>C
DNA change (hg38) -
Published as ACKR1(NM_001122951.3):c.-111T>C
ISCN -
DB-ID DARC_000001 See all 2 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) 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 2022-05-09 15:40:45 +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     
DARC NM_002036.3 -/. - c.-67T>C r.(?) p.(=)
CADM3 NM_021189.3 -/. - c.*3971T>C r.(=) p.(=)


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