Simple Nucleotide Polymorphisms (dbSNP 150) Found in >= 1% of Samples
 

dbSNP build 150 rs1064261

dbSNP: rs1064261
Position: chr1:11228701-11228701
Band: 1p36.22
Genomic Size: 1
View DNA for this feature (hg38/Human)

Summary: T>C/T (chimp allele displayed first, then '>', then human alleles)
Strand: -
Observed: C/T
Reference allele: C
Chimp allele: T    Chimp strand: -    Chimp position:  chr1:10687866-10687866
Orangutan allele: T    Orangutan strand: +    Orangutan position:  chr1:219116287-219116287
Macaque allele: T    Macaque strand: -    Macaque position:  chr1:10491977-10491977

Classsingle
Validationby-cluster,by-frequency,by-2hit-2allele,by-hapmap,by-1000genomes
Functionsynonymous_variant, nc_transcript_variant
Molecule Type  genomic
Average Heterozygosity  0.382 +/- 0.212
Weight1
Submitter Handles  1000GENOMES, ABI, AFFY, BCM-HGSC-SUB, BCMHGSC_JDW, BGI, BL, BUSHMAN, CANCER-GENOME, CGM_KYOTO, CLINSEQ_SNP, COMPLETE_GENOMICS, CSHL-HAPMAP, DDI, ENSEMBL, EVA-GONL, EVA_DECODE, EVA_EXAC, EVA_FINRISK, EVA_GENOME_DK, EVA_MGP, EVA_SVP, EVA_UK10K_ALSPAC, EVA_UK10K_TWINSUK, GENOMED, GMI, HAMMER_LAB, HGSV, HUMANGENOME_JCVI, HUMAN_LONGEVITY, ILLUMINA, IMCJ-GDT, JDRF_WT_DIL, JJLAB, JMKIDD_LAB, KRIBB_YJKIM, LEE, NHLBI-ESP, PJP, SEATTLESEQ, SI_EXO, SSAHASNP, SSMP, TISHKOFF, TOPMED, USC_VALOUEV, WEILL_CORNELL_DGM, WIPGA, WI_SSAHASNP
Allele Frequencies  C: 25.879% (32691 / 126323); T: 74.121% (93632 / 126323)

Miscellaneous properties annotated by dbSNP:
Minor Allele Frequency is at least 5% in all populations assayed
Quality check: Different genotypes have been submitted for the same individual

Coding annotations by dbSNP: