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Select item 10796101.

rs1079610 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:86662359 (GRCh38)
10:88422116 (GRCh37)
Canonical SPDI:: NC_000010.11:86662358:C:A,NC_000010.11:86662358:C:T
Gene:: OPN4 (Varview), LOC105378409 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.3445342/79883 (ALFA)
C=0.1481481/8 (Siberian)
C=0.175/7 (GENOME_DK)
C=0.1888646/346 (Korea1K)
C=0.1906276/1379 (Korea4K)
C=0.1992188/102 (SGDP_PRJ)
C=0.2021977/15659 (TOMMO)
C=0.2044369/599 (KOREAN)
C=0.222561/73 (HapMap)
C=0.244847/1568 (1000Genomes_30X)
C=0.2468051/1236 (1000Genomes)
C=0.2548969/19780 (PAGE_STUDY)
C=0.2714808/19918 (ExAC)
C=0.2982772/78951 (TOPMED)
C=0.3022899/45069 (GnomAD_genomes)
C=0.312943/4062 (GoESP)
C=0.3148148/68 (Qatari)
C=0.3174107/1422 (Estonian)
C=0.343909/473139 (GnomAD_exomes)
C=0.345/207 (NorthernSweden)
C=0.3466934/346 (GoNL)
C=0.3619616/1395 (ALSPAC)
C=0.3778317/1401 (TWINSUK)
C=0.4400749/235 (MGP)
HGVS:: NC_000010.11:g.86662359C>A, NC_000010.11:g.86662359C>T, NC_000010.10:g.88422116C>A, NC_000010.10:g.88422116C>T, NM_033282.4:c.1181C>A, NM_033282.4:c.1181C>T, NM_033282.3:c.1181C>A, NM_033282.3:c.1181C>T, NM_001030015.3:c.1214C>A, NM_001030015.3:c.1214C>T, NM_001030015.2:c.1214C>A, NM_001030015.2:c.1214C>T, XM_017016955.2:c.1214C>A, XM_017016955.2:c.1214C>T, XM_017016955.1:c.1214C>A, XM_017016955.1:c.1214C>T, XM_017016956.2:c.1181C>A, XM_017016956.2:c.1181C>T, XM_017016956.1:c.1181C>A, XM_017016956.1:c.1181C>T, NP_150598.1:p.Thr394Asn, NP_150598.1:p.Thr394Ile, NP_001025186.1:p.Thr405Asn, NP_001025186.1:p.Thr405Ile, XP_016872444.1:p.Thr405Asn, XP_016872444.1:p.Thr405Ile, XP_016872445.1:p.Thr394Asn, XP_016872445.1:p.Thr394Ile

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