chr21:31667359:T>C Detail (hg38) (SOD1)

Information

Genome

Assembly Position
hg19 chr21:33,039,672-33,039,672 View the variant detail on this assembly version.
hg38 chr21:31,667,359-31,667,359

HGVS

Type Transcript Protein
RefSeq NM_000454.4:c.341T>C NP_000445.1:p.Ile114Thr
Ensemble ENST00000270142.11:c.341T>C ENST00000270142.11:p.Ile114Thr
ENST00000389995.4:c.284T>C ENST00000389995.4:p.Ile95Thr
Summary

MGeND

Clinical significance Pathogenic
Variant entry 2
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 147450 OMIM
HGNC 11179 HGNC
Ensembl ENSG00000142168 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv235885478 TogoVar
COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
Pathogenic amyotrophic lateral sclerosis germline MGS000009
(TMGS000039)
Shoji Tsuji Tokyo University
Pathogenic amyotrophic lateral sclerosis unknown MGS000001
(TMGS000162)
Kenjiro Kosaki Keio University
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic Likely pathogenic 2024-01-21 criteria provided, multiple submitters, no conflicts amyotrophic lateral sclerosis type 1 germline Detail
Pathogenic 2021-06-24 criteria provided, multiple submitters, no conflicts not provided germline unknown Detail
Pathogenic 2016-08-31 criteria provided, single submitter motor neuron disease unknown Detail
Pathogenic 2024-02-16 criteria provided, single submitter SOD1-related disorder germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.520 AMYOTROPHIC LATERAL SCLEROSIS 1 NA CLINVAR Detail
0.438 amyotrophic lateral sclerosis A patient is described with a 20 year duration of motor neuron disease, with cli... BeFree 7673954 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000454.5(SOD1):c.341T>C (p.Ile114Thr) AND Amyotrophic lateral sclerosis type 1 ClinVar Detail
NM_000454.5(SOD1):c.341T>C (p.Ile114Thr) AND not provided ClinVar Detail
NM_000454.5(SOD1):c.341T>C (p.Ile114Thr) AND Motor neuron disease ClinVar Detail
NM_000454.5(SOD1):c.341T>C (p.Ile114Thr) AND SOD1-related disorder ClinVar Detail
NA DisGeNET Detail
A patient is described with a 20 year duration of motor neuron disease, with clinical features of AL... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs121912441 dbSNP
Genome
hg38
Position
chr21:31,667,359-31,667,359
Variant Type
snv
Reference Allele
T
Alternative Allele
C
Genome browser