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Select item 3860141.

rs386014 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:29926852 (GRCh38)
6:29894629 (GRCh37)
Canonical SPDI:: NC_000006.12:29926851:G:C
Gene:: HCG4B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.032972/535 (ALFA)
C=0./0 (PRJEB36033)
C=0.000044/3 (TOMMO)
C=0.007205/20 (KOREAN)
C=0.009194/63 (Korea4K)
C=0.018692/4 (Qatari)
C=0.019737/6 (HapMap)
C=0.020478/12 (NorthernSweden)
C=0.025/1 (GENOME_DK)
C=0.031949/160 (1000Genomes)
C=0.033708/18 (MGP)
C=0.034822/223 (1000Genomes_30X)
C=0.036784/5175 (GnomAD_genomes)
C=0.041051/34607 (GnomAD_exomes)
G=0.392857/11 (SGDP_PRJ)
G=0.5/1 (Siberian)
HGVS:: NC_000006.12:g.29926852G>C, NC_000006.11:g.29894629G>C, NG_015982.3:g.294G>C, NT_113891.3:g.1408203G>C, NT_113891.2:g.1408309G>C, NT_167248.2:g.1183641G>C, NT_167248.1:g.1189237G>C, NT_167245.2:g.1184006G>C, NT_167245.1:g.1189591G>C, NT_167249.2:g.1226542G>C, NT_167249.1:g.1225840G>C, NT_167246.2:g.1183216C>G, NT_167246.1:g.1188836C>G, NT_167244.2:g.1186529G>C, NW_003871063.1:g.162706G>C, NT_167244.1:g.1136445G>C, NR_001317.3:n.364C>G, NR_001317.2:n.364C>G

Supplemental Content

386014[uid] (1)
SNP
13306584[uid] (1)
SNP
Homo sapiens ribosomal protein S10 (RPS10), transcript variant 2, mRNA
Homo sapiens ribosomal protein S10 (RPS10), transcript variant 2, mRNA
gi|1390016880|ref|NM_001014.5|

Nucleotide
Synthetic construct Homo sapiens ribosomal protein S10, mRNA (cDNA clone MGC:888...
Synthetic construct Homo sapiens ribosomal protein S10, mRNA (cDNA clone MGC:88819 IMAGE:5517455), complete cds
gi|49256435|gb|BC073799.1|

Nucleotide
Homo sapiens ribosomal protein S10, mRNA (cDNA clone MGC:88633 IMAGE:6305105), c...
Homo sapiens ribosomal protein S10, mRNA (cDNA clone MGC:88633 IMAGE:6305105), complete cds
gi|48734771|gb|BC071946.1|

Nucleotide

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dbSNP