Variant #0000334789 (NC_000023.10:g.80532668G>A, NM_030763.2:c.-75556C>T (HMGN5))

Chromosome X
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.80532668G>A
DNA change (hg38) g.81277169G>A
Published as SH3BGRL(NM_003022.2):c.231G>A (p.?), SH3BGRL(NM_003022.3):c.231G>A (p.G77=)
ISCN -
DB-ID SH3BGRL_000005 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) 0.00082 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH3BGRL NM_003022.2 ?/. - c.231G>A r.(?) p.(Gly77=)
HMGN5 NM_030763.2 ?/. - c.-75556C>T r.(?) p.(=)


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