Variant #0000289220 (NC_000002.11:g.198359436T>C, NM_002156.4:c.551A>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.198359436T>C
DNA change (hg38) g.197494712T>C
Published as HSPD1(NM_002156.5):c.551A>G (p.N184S)
ISCN -
DB-ID HSPD1_000001
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) 0.00046 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPE1-MOB4 NM_001202485.1 ?/. - c.-5725T>C r.(?) p.(=)
HSPD1 NM_002156.4 ?/. - c.551A>G r.(?) p.(Asn184Ser)
HSPE1 NM_002157.2 ?/. - c.-5725T>C r.(?) p.(=)


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