View genomic variant #0000005239

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type del
DNA change (genomic) (Relative to hg19 / GRCh37) g.52942176del
Published as -
GERP 6.060
Segregation -
DB-ID NDUFS4_000001 See all 2 reported entries
MSCV MSCV_0005239
dbSNP ID rs121908985
Frequency -
Sources ; ensembl;
Reference 10944442
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.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS4 00000213 NM_002495.2 0000005239 ./. - - c.291del p.(Trp97*) - - - -
NDUFS4 00000212 XM_005248525.1 0000005239 ./. - - c.291del p.(Trp97*) - - - -
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MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None