Variant #0000802748 (NC_000006.11:g.8041405T>C, NM_030810.3:c.-130396A>G (TXNDC5))

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.8041405T>C
DNA change (hg38) -
Published as BLOC1S5(NM_001199322.1):c.100A>G (p.M34V)
ISCN -
DB-ID TXNDC5_000007
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 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 2021-09-17 14:40:49 +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.*160829T>C r.(=) p.(=)
EEF1E1 NM_004280.4 ?/. - c.*38718A>G r.(=) p.(=)
TXNDC5 NM_030810.3 ?/. - c.-130396A>G r.(?) p.(=)
BLOC1S5 NM_201280.2 ?/. - c.292A>G r.(?) p.(Met98Val)
BLOC1S5-TXNDC5 NR_037616.1 ?/. - n.330A>G r.(?) -


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