Variant #0000546908 (NC_000012.11:g.122685139A>G, NM_019887.5:c.*7789T>C (DIABLO))

Chromosome 12
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.122685139A>G
DNA change (hg38) g.122200592A>G
Published as LRRC43(NM_001098519.1):c.1552A>G (p.(Lys518Glu))
ISCN -
DB-ID B3GNT4_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
IL31 NM_001014336.1 -?/. - c.-26420T>C r.(?) p.(=)
DIABLO NM_019887.5 -?/. - c.*7789T>C r.(=) p.(=)
B3GNT4 NM_030765.2 -?/. - c.-3307A>G r.(?) p.(=)
LRRC43 NM_152759.4 -?/. - c.997A>G r.(?) p.(Lys333Glu)


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