Variant #0000535645 (NC_000009.11:g.103054941G>A, NM_014425.3:c.2402G>A (INVS))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.103054941G>A
DNA change (hg38) g.100292659G>A
Published as INVS(NM_014425.4):c.2402G>A (p.G801E), INVS(NM_014425.5):c.2402G>A (p.(Gly801Glu))
ISCN -
DB-ID INVS_000022 See all 3 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) 0.02754 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INVS NM_014425.3 -/. - c.2402G>A r.(?) p.(Gly801Glu)
TEX10 NM_017746.3 -/. - c.*9532C>T r.(=) p.(=)


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