Variant #0000622587 (NC_000011.9:g.124794912C>T, NM_152722.4:c.139G>A (HEPACAM))

Chromosome 11
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.124794912C>T
DNA change (hg38) g.124925016C>T
Published as HEPACAM(NM_152722.5):c.139G>A (p.V47M)
ISCN -
DB-ID HEPACAM_000006
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) 0.00011 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HEPN1 NM_001037558.2 ?/. - c.*4999C>T r.(=) p.(=)
HEPACAM NM_152722.4 ?/. - c.139G>A r.(?) p.(Val47Met)


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