Variant #0000327011 (NC_000002.11:g.53995042G>C, NC_000002.11(NM_016115.4):c.-13-2320C>G (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.53995042G>C
DNA change (hg38) g.53767905G>C
Published as CHAC2(NM_001008708.2):c.19G>C (p.(Gly7Arg))
ISCN -
DB-ID ASB3_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) 0.0001 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHAC2 NM_001008708.2 ?/. - c.19G>C r.(?) p.(Gly7Arg)
GPR75-ASB3 NM_001164165.1 ?/. - c.102-2320C>G r.(=) p.(=)
GPR75 NM_006794.3 ?/. - c.*85229C>G r.(=) p.(=)
ERLEC1 NM_015701.4 ?/. - c.-19306G>C r.(?) p.(=)
ASB3 NM_016115.4 ?/. - c.-13-2320C>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.