rs737111 - SNP

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Select item 7371111.

rs737111 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 12:91055578 (GRCh38)
12:91449355 (GRCh37)
Canonical SPDI:: NC_000012.12:91055577:A:C
Gene:: KERA (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (HapMap)
HGVS:: NC_000012.12:g.91055578A>C, NC_000012.11:g.91449355A>C, NG_021223.1:g.7777T>G, NM_007035.3:c.704T>G, NM_007035.4:c.704T>G, NP_008966.1:p.Val235Gly

Select item 3866096322.

rs386609632 has merged into rs737111 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 12:91055578 (GRCh38)
12:91449355 (GRCh37)
Canonical SPDI:: NC_000012.12:91055577:A:C
Gene:: KERA (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (HapMap)
HGVS:: NC_000012.12:g.91055578A>C, NC_000012.11:g.91449355A>C, NG_021223.1:g.7777T>G, NM_007035.3:c.704T>G, NM_007035.4:c.704T>G, NP_008966.1:p.Val235Gly