View genomic variant #0000019378

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207012533C>T
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000037
MSCV MSCV_0019378
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS1 00000204 NM_001199981.1 0000019378 ./. - - c.256G>A p.(Ala86Thr) - - - -
NDUFS1 00000202 NM_001199982.1 0000019378 ./. - - c.31G>A p.(Ala11Thr) - - - -
NDUFS1 00000203 NM_001199983.1 0000019378 ./. - - c.193G>A p.(Ala65Thr) - - - -
NDUFS1 00000206 NM_001199984.1 0000019378 ./. - - c.406G>A p.(Ala136Thr) - - - -
NDUFS1 00000205 NM_005006.6 0000019378 ./. - - c.364G>A p.(Ala122Thr) - - - -
Legend  


Error in query:
SELECT DISTINCT t2.RCVaccession2, t1.chromosome, t1.position_g_start, t2.INFO , t3.RCVaccession, t3.Chromosome, t3.Start, t3.Stop FROM gb_mito.mito5_variants AS t1, gb_exome.clinvar_vcf_latest AS t2 LEFT JOIN gb_exome.clinvar_variation_v2_latest AS t3 ON (t3.variantID= t2.ID AND t3.assembly ='GRCh37') WHERE t1.id='0000019378' AND t2.chr = t1.chromosome AND ( (t1.position_g_start = t2.position OR t1.position_g_end = t2.position) OR ( t1.`VariantOnGenome/DNA` NOT LIKE '%>%' AND ABS(t1.position_g_start - t2.position) =1) ) ;
Query execution was interrupted, maximum statement execution time exceeded