rs1135866 - SNP

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Select item 11358661.

rs1135866 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:90971864 (GRCh38)
12:91365641 (GRCh37)
Canonical SPDI:: NC_000012.12:90971863:A:G
Gene:: EPYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (HapMap)
HGVS:: NC_000012.12:g.90971864A>G, NC_000012.11:g.91365641A>G, NM_004950.5:c.638T>C, NM_004950.4:c.638T>C, XM_011538008.2:c.455T>C, XM_011538008.1:c.455T>C, NP_004941.2:p.Leu213Ser, XP_011536310.1:p.Leu152Ser

Select item 3865181082.

rs386518108 has merged into rs1135866 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:90971864 (GRCh38)
12:91365641 (GRCh37)
Canonical SPDI:: NC_000012.12:90971863:A:G
Gene:: EPYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (HapMap)
HGVS:: NC_000012.12:g.90971864A>G, NC_000012.11:g.91365641A>G, NM_004950.5:c.638T>C, NM_004950.4:c.638T>C, XM_011538008.2:c.455T>C, XM_011538008.1:c.455T>C, NP_004941.2:p.Leu213Ser, XP_011536310.1:p.Leu152Ser