Variant #0000339611 (NC_000002.11:g.198363504A>G, NM_002156.4:c.69T>C (HSPD1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.198363504A>G
DNA change (hg38) g.197498780A>G
Published as -
ISCN -
DB-ID HSPD1_000009
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) 0.17201 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPE1-MOB4 NM_001202485.1 -/. - c.-1657A>G r.(?) p.(=)
HSPD1 NM_002156.4 -/. - c.69T>C r.(?) p.(Thr23=)
HSPE1 NM_002157.2 -/. - c.-1657A>G r.(?) p.(=)
MOB4 NM_015387.4 -/. - c.-17307A>G r.(?) p.(=)


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