Variant #0000285972 (NC_000019.9:g.49519873G>C, NM_000894.2:c.114C>G (LHB))

Chromosome 19
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.49519873G>C
DNA change (hg38) g.49016616G>C
Published as LHB(NM_000894.2):c.114C>G (p.V38=), LHB(NM_000894.3):c.114C>G (p.V38=)
ISCN -
DB-ID LHB_000003 See all 2 reported entries
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) 0.56366 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHB NM_000894.2 -/. - c.114C>G r.(?) p.(Val38=)
RUVBL2 NM_006666.1 -/. - c.*774G>C r.(=) p.(=)


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