Variant #0000948781 (NC_000006.11:g.8064583A>T, NM_030810.3:c.-153574T>A (TXNDC5))

Chromosome 6
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.8064583A>T
DNA change (hg38) -
Published as BLOC1S5(NM_201280.3):c.27T>A (p.P9=)
ISCN -
DB-ID TXNDC5_000012
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) 0.00013 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMP6 NM_001718.4 -?/. - c.*184007A>T r.(=) p.(=)
EEF1E1 NM_004280.4 -?/. - c.*15540T>A r.(=) p.(=)
TXNDC5 NM_030810.3 -?/. - c.-153574T>A r.(?) p.(=)
BLOC1S5 NM_201280.2 -?/. - c.27T>A r.(?) p.(=)
BLOC1S5-TXNDC5 NR_037616.1 -?/. - n.65T>A r.(?) -


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