Variant #0000924580 (NC_000006.11:g.8016071G>T, NM_030810.3:c.-105062C>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.8016071G>T
DNA change (hg38) -
Published as BLOC1S5(NM_001199322.1):c.193-10C>A
ISCN -
DB-ID TXNDC5_000009
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) 0.00266 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 2023-04-16 21:50:28 +02:00 (CEST)
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.*135495G>T r.(=) p.(=)
EEF1E1 NM_004280.4 -?/. - c.*64052C>A r.(=) p.(=)
TXNDC5 NM_030810.3 -?/. - c.-105062C>A r.(?) p.(=)
BLOC1S5 NM_201280.2 -?/. - c.385-10C>A r.(=) p.(=)
BLOC1S5-TXNDC5 NR_037616.1 -?/. - n.422+10529C>A r.(?) -


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