Variant #0000524821 (NC_000005.9:g.149412023G>T, NM_014983.2:c.1840G>T (HMGXB3))

Chromosome 5
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.149412023G>T
DNA change (hg38) g.150032460G>T
Published as HMGXB3(NM_014983.2):c.1840G>T (p.G614C)
ISCN -
DB-ID HMGXB3_000003
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     
HMGXB3 NM_014983.2 ?/. - c.1840G>T r.(?) p.(Gly614Cys)
TIGD6 NM_030953.3 ?/. - c.-32068C>A r.(?) p.(=)


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