Variant #0000532721 (NC_000007.13:g.81392140G>A, NM_000601.4:c.137C>T (HGF))

Chromosome 7
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.81392140G>A
DNA change (hg38) g.81762824G>A
Published as HGF(NM_000601.4):c.137C>T (p.(Ala46Val)), HGF(NM_000601.5):c.137C>T (p.A46V), HGF(NM_000601.6):c.137C>T (p.A46V)
ISCN -
DB-ID HGF_000015 See all 3 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) 0.00177 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGF NM_000601.4 ?/. - c.137C>T r.(?) p.(Ala46Val)


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