Variant #0000884666 (NC_000002.11:g.198353797T>C, NM_002156.4:c.1144A>G (HSPD1))

Chromosome 2
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.198353797T>C
DNA change (hg38) -
Published as HSPD1(NM_002156.5):c.1144A>G (p.T382A)
ISCN -
DB-ID HSPD1_000022
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPE1-MOB4 NM_001202485.1 ?/. - c.-11364T>C r.(?) p.(=)
HSPD1 NM_002156.4 ?/. - c.1144A>G r.(?) p.(Thr382Ala)
HSPE1 NM_002157.2 ?/. - c.-11364T>C r.(?) p.(=)


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