NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss5237042449           
Submitter
HandleEVA
Submitter SNP IDPRJEB41091_8_42731922_C_T
RefSNP(rs#)clustering in process
Submitted Batch IDPRJEB41688
Submitted DateMar 10, 2021
Publication CitedN.D.
First entry to dbSNPMar 10 2021 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodEXOME SEQUENCING
Ascertainment Samplesize410
PopulationPRJEB41688
Allele
Observed AlleleC/T
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|ss5237042449|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 ATAACGGAGA ATGGGAAATA CTGAA
 Y
 GCAAAGGGGA TGAAGGGGAA CAGAA

  Submitted Frequency for ss5237042449 back to top
There is no frequency submission for ss5237042449.


  dbSNP summary of Genotypes for ss5237042449 back to top
No sufficient data to compute Hardy-weinberg probability for ss5237042449.


  Submitted individual genotype for ss5237042449 back to top
There is no individual genotype data for ss5237042449.