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Select item 349580841.

rs34958084 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:167383862 (GRCh38)
1:167353099 (GRCh37)
Canonical SPDI:: NC_000001.11:167383861:C:T
Gene:: POU2F1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.0035142/228 (ALFA)
T=0.0006797/952 (GnomAD_exomes)
T=0.0015974/1 (Chileans)
T=0.0019939/242 (ExAC)
T=0.0046296/1 (Qatari)
T=0.0067547/1008 (GnomAD_genomes)
T=0.0073392/47 (1000Genomes_30X)
T=0.0073882/37 (1000Genomes)
T=0.007454/1973 (TOPMED)
T=0.0076888/100 (GoESP)
T=0.0115118/906 (PAGE_STUDY)
T=0.0238095/17 (HapMap)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.167383862C>T, NC_000001.10:g.167353099C>T, NM_002697.4:c.724C>T, NM_002697.3:c.724C>T, XM_011509654.4:c.655C>T, XM_011509654.3:c.655C>T, XM_011509654.2:c.655C>T, XM_011509654.1:c.655C>T, XM_017001508.3:c.733C>T, XM_017001508.2:c.733C>T, XM_017001508.1:c.733C>T, XM_011509655.2:c.733C>T, XM_011509655.1:c.733C>T, NM_001198783.2:c.691C>T, NM_001198783.1:c.691C>T, NR_037163.2:n.837C>T, NR_037163.1:n.837C>T, XM_011509653.2:c.733C>T, XM_011509653.1:c.733C>T, NM_001198786.2:c.535C>T, NM_001198786.1:c.535C>T, XM_047422869.1:c.655C>T, XM_047422877.1:c.724C>T, NM_001365848.1:c.649C>T, NM_001365849.1:c.649C>T, XM_047422875.1:c.655C>T

dbSNP