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Submitted SNP(ss) Details: ss3645007211           
Submitter
HandleILLUMINA
Submitter SNP IDHumanCoreExome-24v1-0_A_MitoA10551G-0_T_F_1852726286
RefSNP(rs#)clustering in process
Submitted Batch IDHumanCoreExome-24v1-0_A
Submitted DateJan 30, 2018
Publication CitedN.D.
First entry to dbSNPJan 30 2018 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize547644
PopulationN.D.
Allele
Observed AlleleA/G
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Homozygote Detected
PCR Confirmed
In Expressed Sequence
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3645007211|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 TACTAGTATA TCGCTCACAC CTCAT
 R
 TCCTCCCTAC TATGCCTAGA AGGAA

  Submitted Frequency for ss3645007211 back to top
There is no frequency submission for ss3645007211.


  dbSNP summary of Genotypes for ss3645007211 back to top
No sufficient data to compute Hardy-weinberg probability for ss3645007211.


  Submitted individual genotype for ss3645007211 back to top
There is no individual genotype data for ss3645007211.