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Select item 30805991.

rs3080599 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 12:9074098 (GRCh38)
12:9226694 (GRCh37)
Canonical SPDI:: NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:9074087:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: A2M (Varview), KLRG1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.3524/1765 (1000Genomes)
HGVS:: NC_000012.12:g.9074098_9074107del, NC_000012.12:g.9074099_9074107del, NC_000012.12:g.9074101_9074107del, NC_000012.12:g.9074102_9074107del, NC_000012.12:g.9074103_9074107del, NC_000012.12:g.9074104_9074107del, NC_000012.12:g.9074105_9074107del, NC_000012.12:g.9074106_9074107del, NC_000012.12:g.9074107del, NC_000012.12:g.9074107dup, NC_000012.12:g.9074106_9074107dup, NC_000012.12:g.9074105_9074107dup, NC_000012.12:g.9074104_9074107dup, NC_000012.11:g.9226694_9226703del, NC_000012.11:g.9226695_9226703del, NC_000012.11:g.9226697_9226703del, NC_000012.11:g.9226698_9226703del, NC_000012.11:g.9226699_9226703del, NC_000012.11:g.9226700_9226703del, NC_000012.11:g.9226701_9226703del, NC_000012.11:g.9226702_9226703del, NC_000012.11:g.9226703del, NC_000012.11:g.9226703dup, NC_000012.11:g.9226702_9226703dup, NC_000012.11:g.9226701_9226703dup, NC_000012.11:g.9226700_9226703dup, NG_011717.2:g.46866_46875del, NG_011717.2:g.46867_46875del, NG_011717.2:g.46869_46875del, NG_011717.2:g.46870_46875del, NG_011717.2:g.46871_46875del, NG_011717.2:g.46872_46875del, NG_011717.2:g.46873_46875del, NG_011717.2:g.46874_46875del, NG_011717.2:g.46875del, NG_011717.2:g.46875dup, NG_011717.2:g.46874_46875dup, NG_011717.2:g.46873_46875dup, NG_011717.2:g.46872_46875dup

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