Variant #0000611753 (NC_000009.11:g.103055081T>G, NM_014425.3:c.2542T>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.103055081T>G
DNA change (hg38) g.100292799T>G
Published as INVS(NM_001318381.1):c.2254T>G (p.L752V)
ISCN -
DB-ID TEX10_000018
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 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.2542T>G r.(?) p.(Leu848Val)
TEX10 NM_017746.3 -?/. - c.*9392A>C r.(=) p.(=)


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