Variant #0000613458 (NC_000011.9:g.57506518A>G, NC_000011.9(NM_015959.3):c.614+7A>G (TMX2))

Chromosome 11
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.57506518A>G
DNA change (hg38) g.57739046A>G
Published as TMX2(NM_015959.4):c.614+7A>G
ISCN -
DB-ID C11orf31_000014
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) 3.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 -?/. - c.-23287A>G r.(?) p.(=)
BTBD18 NM_001145101.1 -?/. - c.*5088T>C r.(=) p.(=)
TMX2 NM_015959.3 -?/. - c.614+7A>G r.(=) p.(=)
C11orf31 NM_170746.2 -?/. - c.-2550A>G r.(?) p.(=)
TMX2-CTNND1 NR_037646.1 -?/. - n.346+1378A>G r.(?) -


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