View genomic variant #0000019360

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207003230C>T
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000027
MSCV MSCV_0019360
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01369 View details
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 0000019360 ./. - - c.1263G>A p.(=) - - - -
NDUFS1 00000202 NM_001199982.1 0000019360 ./. - - c.1038G>A p.(=) - - - -
NDUFS1 00000203 NM_001199983.1 0000019360 ./. - - c.1200G>A p.(=) - - - -
NDUFS1 00000206 NM_001199984.1 0000019360 ./. - - c.1413G>A p.(=) - - - -
NDUFS1 00000205 NM_005006.6 0000019360 ./. - - c.1371G>A p.(=) - - - -
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='0000019360' 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