Variant #0000861320 (NC_000009.11:g.103060213T>G, NC_000009.11(NM_014425.3):c.3017-5T>G (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.103060213T>G
DNA change (hg38) -
Published as INVS(NM_014425.4):c.3017-5T>G, INVS(NM_014425.5):c.3017-5T>G
ISCN -
DB-ID TEX10_000013 See all 4 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) 0.00279 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.3017-5T>G r.spl? p.?
TEX10 NM_017746.3 -?/. - c.*4260A>C r.(=) p.(=)


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