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Select item 115451301.

rs11545130 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:39087097 (GRCh38)
22:39483102 (GRCh37)
Canonical SPDI:: NC_000022.11:39087096:C:T
Gene:: APOBEC3G (Varview)
Functional Consequence:: genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.0023275/417 (ALFA)
T=0./0 (TWINSUK)
T=0.0005189/2 (ALSPAC)
T=0.0009627/1349 (GnomAD_exomes)
T=0.002534/307 (ExAC)
T=0.0077875/39 (1000Genomes)
T=0.0081865/1222 (GnomAD_genomes)
T=0.0084322/54 (1000Genomes_30X)
T=0.0092221/2441 (TOPMED)
T=0.0093034/121 (GoESP)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000022.11:g.39087097C>T, NC_000022.10:g.39483102C>T, NM_021822.4:c.1111C>T, NM_021822.3:c.1111C>T, NM_001349437.2:c.910C>T, NM_001349437.1:c.910C>T, NM_001349436.1:c.1078C>T

Supplemental Content

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