Simple Nucleotide Polymorphisms (dbSNP 150) Found in >= 1% of Samples
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dbSNP build 150 rs1057079
dbSNP: rs1057079
Position: chr1:11145001-11145001
Band: 1p36.22
Genomic Size: 1
View DNA for this feature (hg38/Human)
Summary: G>A/G (chimp allele displayed first, then '>', then human alleles)
Strand: -
Observed: A/G
Class | single |
Validation | by-cluster,by-frequency,by-submitter,by-2hit-2allele,by-hapmap,by-1000genomes |
Function | synonymous_variant, intron_variant, nc_transcript_variant |
Molecule Type | genomic |
Average Heterozygosity | 0.437 +/- 0.166 |
Weight | 1 |
Submitter Handles | 1000GENOMES, ABI, AFFY, BCM-HGSC-SUB, BCMHGSC_JDW, BGI, BL, CANCER-GENOME, 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, HGSV, HUMAN_LONGEVITY, ILLUMINA, IMCJ-GDT, JDRF_WT_DIL, JJLAB, JMKIDD_LAB, KRIBB_YJKIM, KWOK, LEE, NHLBI-ESP, PERLEGEN, PJP, SC_JCM, SC_SNP, SEATTLESEQ, SI_EXO, SSAHASNP, SSMP, TISHKOFF, TOPMED, USC_VALOUEV, WEILL_CORNELL_DGM, WIPGA, YUSUKE |
Allele Frequencies | A: 67.276% (85039 / 126404); G: 32.724% (41365 / 126404) |
Miscellaneous properties annotated by dbSNP:
Minor Allele Frequency is at least 5% in at least one population assayed
Coding annotations by dbSNP:
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