Variant #0000964271 (NC_000006.11:g.7910948_7910950del, NM_030810.3:c.76_78del (TXNDC5))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7910948_7910950del
DNA change (hg38) -
Published as TXNDC5(NM_030810.5):c.76_78delCTG (p.L26del)
ISCN -
DB-ID TXNDC5_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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +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.*30372_*30374del r.(=) p.(=)
TXNDC5 NM_030810.3 -/. - c.76_78del r.(?) p.(Leu26del)
BLOC1S5 NM_201280.2 -/. - c.*104948_*104950del r.(=) p.(=)
BLOC1S5-TXNDC5 NR_037616.1 -/. - n.423-5978_423-5976del r.(?) -


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