Variant #0000894246 (NC_000017.10:g.72943106A>G, NM_030630.2:c.*4559T>C (HID1))

Chromosome 17
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.72943106A>G
DNA change (hg38) -
Published as OTOP3(NM_001272005.1):c.1102A>G (p.(Met368Val))
ISCN -
DB-ID OTOP3_000002
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 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HID1 NM_030630.2 ?/. - c.*4559T>C r.(=) p.(=)
OTOP3 NM_178233.1 ?/. - c.1156A>G r.(?) p.(Met386Val)


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