Variant #0000321177 (NC_000001.10:g.186034508T>C, NM_031935.2:c.7652T>C (HMCN1))

Chromosome 1
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.186034508T>C
DNA change (hg38) g.186065376T>C
Published as HMCN1(NM_031935.2):c.7652T>C (p.(Leu2551Ser)), HMCN1(NM_031935.3):c.7652T>C (p.L2551S)
ISCN -
DB-ID HMCN1_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) 0.00112 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMCN1 NM_031935.2 ?/. - c.7652T>C r.(?) p.(Leu2551Ser)


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