Variant #0000611751 (NC_000009.11:g.102991972A>G, NM_014425.3:c.478A>G (INVS))

Chromosome 9
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.102991972A>G
DNA change (hg38) g.100229690A>G
Published as INVS(NM_001318381.1):c.190A>G (p.N64D)
ISCN -
DB-ID TEX10_000016
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 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +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.478A>G r.(?) p.(Asn160Asp)
TEX10 NM_017746.3 ?/. - c.*72501T>C r.(=) p.(=)


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