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Select item 97115031.

rs9711503 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:233757551 (GRCh38)
2:234666197 (GRCh37)
Canonical SPDI:: NC_000002.12:233757550:T:C
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview), UGT1A4 (Varview), UGT1A3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.03311/421 (ALFA)
C=0.0034/57 (TOMMO)
C=0.01057/19 (Korea1K)
C=0.01186/827 (GnomAD)
C=0.08755/239 (KOREAN)
C=0.19907/43 (Qatari)
T=0.5/3 (Siberian)
T=0.5/67 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233757551T>C, NC_000002.11:g.234666197T>C, NG_002601.2:g.172808T>C, NG_033238.1:g.2279T>C

Supplemental Content

9711503[uid] (1)
SNP
Babesia microti strain RI mitochondria, complete genome
Babesia microti strain RI mitochondria, complete genome
gi|1135449590|emb|LN871600.2|

Nucleotide
Babesia microti strain RI chromosome I, complete genome
Babesia microti strain RI chromosome I, complete genome
gi|399215784|emb|FO082871.1|

Nucleotide
NS1 [African horse sickness virus 4]
NS1 [African horse sickness virus 4]
gi|873290891|gb|AKP39984.1|

Protein

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