Variant #0000256254 (NC_000006.11:g.24667084A>T, NM_016614.2:c.7T>A (TDP2))

Chromosome 6
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.24667084A>T
DNA change (hg38) g.24666856A>T
Published as TDP2(NM_016614.2):c.7T>A (p.L3M)
ISCN -
DB-ID TDP2_000003
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TDP2 NM_016614.2 ?/. - c.7T>A r.(?) p.(Leu3Met)
ACOT13 NM_018473.3 ?/. - c.-408A>T r.(?) p.(=)
C6orf62 NM_030939.4 ?/. - c.*39281T>A r.(=) p.(=)


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