Variant #0000981339 (NC_000015.9:g.63978588T>C, NM_003922.3:c.6195A>G (HERC1))

Chromosome 15
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.63978588T>C
DNA change (hg38) -
Published as HERC1(NM_003922.3):c.6195A>G (p.T2065=), HERC1(NM_003922.4):c.6195A>G (p.(Thr2065=))
ISCN -
DB-ID HERC1_000089 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) 0.00075 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HERC1 NM_003922.3 -?/. - c.6195A>G r.(?) p.(Thr2065=)


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