rs193328 - SNP

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Select item 1933281.

rs193328 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:9789339 (GRCh38)
11:9810886 (GRCh37)
Canonical SPDI:: NC_000011.10:9789338:G:A
Gene:: SBF2 (Varview), SBF2-AS1 (Varview), LOC105369149 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (HapMap)
HGVS:: NC_000011.10:g.9789339G>A, NC_000011.9:g.9810886G>A, NG_008074.1:g.509869C>T, NM_030962.4:c.4702C>T, NM_030962.3:c.4702C>T, NM_001386339.1:c.4798C>T, NM_001386342.1:c.4573C>T, XM_047427657.1:c.*6C>T

Select item 3952572.

rs395257 has merged into rs193328 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:9789339 (GRCh38)
11:9810886 (GRCh37)
Canonical SPDI:: NC_000011.10:9789338:G:A
Gene:: SBF2 (Varview), SBF2-AS1 (Varview), LOC105369149 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (HapMap)
HGVS:: NC_000011.10:g.9789339G>A, NC_000011.9:g.9810886G>A, NG_008074.1:g.509869C>T, NM_030962.4:c.4702C>T, NM_030962.3:c.4702C>T, NM_001386339.1:c.4798C>T, NM_001386342.1:c.4573C>T, XM_047427657.1:c.*6C>T