rs1042284 - SNP

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Select item 10422841.

rs1042284 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:847933 (GRCh38)
19:847933 (GRCh37)
Canonical SPDI:: NC_000019.10:847932:C:T
Gene:: PRTN3 (Varview)
Functional Consequence:: coding_sequence_variant,3_prime_UTR_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.847933C>T, NC_000019.9:g.847933C>T, NG_009627.1:g.643C>T, NT_187622.1:g.26776C>T, NM_002777.4:c.735C>T, NM_002777.3:c.735C>T, XM_011528136.2:c.*163C>T

Select item 31817272.

rs3181727 has merged into rs1042284 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:847933 (GRCh38)
19:847933 (GRCh37)
Canonical SPDI:: NC_000019.10:847932:C:T
Gene:: PRTN3 (Varview)
Functional Consequence:: coding_sequence_variant,3_prime_UTR_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.847933C>T, NC_000019.9:g.847933C>T, NG_009627.1:g.643C>T, NT_187622.1:g.26776C>T, NM_002777.4:c.735C>T, NM_002777.3:c.735C>T, XM_011528136.2:c.*163C>T