Variant #0000327012 (NC_000002.11:g.54080338G>A, NM_016115.4:c.-66394C>T (ASB3))

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.54080338G>A
DNA change (hg38) g.53853201G>A
Published as GPR75(NM_006794.3):c.1556C>T (p.(Thr519Ile))
ISCN -
DB-ID GPR75_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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     
CHAC2 NM_001008708.2 ?/. - c.*78676G>A r.(=) p.(=)
GPR75-ASB3 NM_001164165.1 ?/. - c.101+6627C>T r.(=) p.(=)
GPR75 NM_006794.3 ?/. - c.1556C>T r.(?) p.(Thr519Ile)
ERLEC1 NM_015701.4 ?/. - c.*35232G>A r.(=) p.(=)
ASB3 NM_016115.4 ?/. - c.-66394C>T r.(?) p.(=)


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