View genomic variant #0000000844

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.198363487T>C
Published as -
GERP 4.870
Segregation -
DB-ID HSPD1_000001 See all 2 reported entries
MSCV MSCV_0000844
dbSNP ID rs72466451
Frequency -
Sources ; clinVar; Ensembl;
Reference 18571143
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
HSPD1 00000157 NM_002156.4 0000000844 +/+ - 2/3 c.86A>G p.(Asp29Gly) benign(0.021) missense_variant - deleterious(0.03)
HSPD1 00000156 NM_199440.1 0000000844 +/+ - 2/3 c.86A>G p.(Asp29Gly) benign(0.021) missense_variant - deleterious(0.03)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000019113;
Chromosome 2:198363487..198363487
ClinVar Allele ID 32597
Disease database name and identifier MONDO:MONDO:0012824, MedGen:C2677109, OMIM:612233, Orphanet:280270, Orphanet:280288
ClinVar preferred disease name Hypomyelinating leukodystrophy 4
HGVS variant names NC 000002.11:g.198363487T>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA127253|OMIM:118190.0002|UniProtKB:P10809#VAR 054785
Gene symbol:Gene id. HSPD1:3329
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 72466451
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None