Variant #0000332719 (NC_000009.11:g.102866870G>A, NM_014425.3:c.67G>A (INVS))

Chromosome 9
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.102866870G>A
DNA change (hg38) g.100104588G>A
Published as INVS(NM_014425.3):c.67G>A (p.(Val23Ile)), INVS(NM_014425.4):c.67G>A (p.V23I), INVS(NM_014425.5):c.67G>A (p.V23I)
ISCN -
DB-ID INVS_000003 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) 0.0003 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INVS NM_014425.3 -?/. - c.67G>A r.(?) p.(Val23Ile)
TEX10 NM_017746.3 -?/. - c.*197603C>T r.(=) p.(=)


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