Variant #0000256375 (NC_000009.11:g.103004888A>G, NM_014425.3:c.833A>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.103004888A>G
DNA change (hg38) g.100242606A>G
Published as INVS(NM_014425.4):c.833A>G (p.N278S)
ISCN -
DB-ID INVS_000011
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INVS NM_014425.3 ?/. - c.833A>G r.(?) p.(Asn278Ser)
TEX10 NM_017746.3 ?/. - c.*59585T>C r.(=) p.(=)


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