Variant #0000281278 (NC_000015.9:g.28478316T>G, NM_004667.5:c.4651A>C (HERC2))

Chromosome 15
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.28478316T>G
DNA change (hg38) g.28233170T>G
Published as HERC2(NM_004667.5):c.4651A>C (p.I1551L), HERC2(NM_004667.6):c.4651A>C (p.I1551L)
ISCN -
DB-ID HERC2_000032 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) 0.00042 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 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     
HERC2 NM_004667.5 ?/. - c.4651A>C r.(?) p.(Ile1551Leu)


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