Variant #0000720268 (NC_000005.9:g.149410364A>G, NM_014983.2:c.1795A>G (HMGXB3))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.149410364A>G
DNA change (hg38) -
Published as HMGXB3(NM_014983.2):c.1795A>G (p.M599V)
ISCN -
DB-ID HMGXB3_000018
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMGXB3 NM_014983.2 -?/. - c.1795A>G r.(?) p.(Met599Val)
TIGD6 NM_030953.3 -?/. - c.-30409T>C r.(?) p.(=)


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