SNP Links for Nucleotide (Select 224586941) - SNP

Links from Nucleotide

Items: 1 to 20 of 1030

<< First< Prev

Page of 52

Next >Last >>

Select item 14868350921.

rs1486835092 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:61639183 (GRCh38)
11:61406655 (GRCh37)
Canonical SPDI:: NC_000011.10:61639182:C:A
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000011.10:g.61639183C>A, NC_000011.9:g.61406655C>A, NR_002775.2:n.3259C>A

Select item 14860790092.

rs1486079009 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:61624996 (GRCh38)
11:61392468 (GRCh37)
Canonical SPDI:: NC_000011.10:61624995:G:A
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000071/10 (GnomAD)
A=0.000125/33 (TOPMED)
A=0.000212/4 (TOMMO)
HGVS:: NC_000011.10:g.61624996G>A, NC_000011.9:g.61392468G>A, NR_002775.2:n.105G>A

Select item 14858269233.

rs1485826923 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:61636808 (GRCh38)
11:61404280 (GRCh37)
Canonical SPDI:: NC_000011.10:61636807:C:A,NC_000011.10:61636807:C:T
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.61636808C>A, NC_000011.10:g.61636808C>T, NC_000011.9:g.61404280C>A, NC_000011.9:g.61404280C>T, NR_002775.2:n.884C>A, NR_002775.2:n.884C>T

Select item 14857499314.

rs1485749931 [Homo sapiens]

Variant type:: DELINS
Alleles:: CAAAGAAA>- [Show Flanks]
Chromosome:: 11:61637748 (GRCh38)
11:61405220 (GRCh37)
Canonical SPDI:: NC_000011.10:61637740:AAAGAAACAAAGAAA:AAAGAAA
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AAAGAAA=0.000084/1 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000011.10:g.61637748_61637755del, NC_000011.9:g.61405220_61405227del, NR_002775.2:n.1824_1831del

Select item 14857030405.

rs1485703040 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:61639258 (GRCh38)
11:61406730 (GRCh37)
Canonical SPDI:: NC_000011.10:61639257:A:G
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.61639258A>G, NC_000011.9:g.61406730A>G, NR_002775.2:n.3334A>G

Select item 14856418676.

rs1485641867 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:61637332 (GRCh38)
11:61404804 (GRCh37)
Canonical SPDI:: NC_000011.10:61637331:G:A,NC_000011.10:61637331:G:T
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.61637332G>A, NC_000011.10:g.61637332G>T, NC_000011.9:g.61404804G>A, NC_000011.9:g.61404804G>T, NR_002775.2:n.1408G>A, NR_002775.2:n.1408G>T

Select item 14852007837.

rs1485200783 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:61638234 (GRCh38)
11:61405706 (GRCh37)
Canonical SPDI:: NC_000011.10:61638233:C:T
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000169/2 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.61638234C>T, NC_000011.9:g.61405706C>T, NR_002775.2:n.2310C>T

Select item 14838626068.

rs1483862606 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 11:61637712 (GRCh38)
11:61405185 (GRCh37)
Canonical SPDI:: NC_000011.10:61637712::G
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.61637712_61637713insG, NC_000011.9:g.61405184_61405185insG, NR_002775.2:n.1788_1789insG

Select item 14834799399.

rs1483479939 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:61636698 (GRCh38)
11:61404170 (GRCh37)
Canonical SPDI:: NC_000011.10:61636697:G:A
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000011.10:g.61636698G>A, NC_000011.9:g.61404170G>A, NR_002775.2:n.774G>A

Select item 148344090310.

rs1483440903 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:61637850 (GRCh38)
11:61405322 (GRCh37)
Canonical SPDI:: NC_000011.10:61637849:G:A,NC_000011.10:61637849:G:T
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000026/7 (TOPMED)
HGVS:: NC_000011.10:g.61637850G>A, NC_000011.10:g.61637850G>T, NC_000011.9:g.61405322G>A, NC_000011.9:g.61405322G>T, NR_002775.2:n.1926G>A, NR_002775.2:n.1926G>T

Select item 148142596411.

rs1481425964 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:61638547 (GRCh38)
11:61406019 (GRCh37)
Canonical SPDI:: NC_000011.10:61638546:T:C
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.61638547T>C, NC_000011.9:g.61406019T>C, NR_002775.2:n.2623T>C

Select item 148096785412.

rs1480967854 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:61637056 (GRCh38)
11:61404528 (GRCh37)
Canonical SPDI:: NC_000011.10:61637055:A:C
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.61637056A>C, NC_000011.9:g.61404528A>C, NR_002775.2:n.1132A>C

Select item 147990692613.

rs1479906926 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:61636792 (GRCh38)
11:61404264 (GRCh37)
Canonical SPDI:: NC_000011.10:61636791:A:G
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.61636792A>G, NC_000011.9:g.61404264A>G, NR_002775.2:n.868A>G

Select item 147981647914.

rs1479816479 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:61638090 (GRCh38)
11:61405562 (GRCh37)
Canonical SPDI:: NC_000011.10:61638089:G:A
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000016/2 (GnomAD)
HGVS:: NC_000011.10:g.61638090G>A, NC_000011.9:g.61405562G>A, NR_002775.2:n.2166G>A

Select item 147935680915.

rs1479356809 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:61637473 (GRCh38)
11:61404945 (GRCh37)
Canonical SPDI:: NC_000011.10:61637472:T:A
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.61637473T>A, NC_000011.9:g.61404945T>A, NR_002775.2:n.1549T>A

Select item 147918653916.

rs1479186539 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:61637127 (GRCh38)
11:61404599 (GRCh37)
Canonical SPDI:: NC_000011.10:61637126:G:A
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.61637127G>A, NC_000011.9:g.61404599G>A, NR_002775.2:n.1203G>A

Select item 147747335717.

rs1477473357 has merged into rs71471834 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:61638132 (GRCh38)
11:61405604 (GRCh37)
Canonical SPDI:: NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:61638126:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
HGVS:: NC_000011.10:g.61638132_61638144del, NC_000011.10:g.61638136_61638144del, NC_000011.10:g.61638137_61638144del, NC_000011.10:g.61638138_61638144del, NC_000011.10:g.61638139_61638144del, NC_000011.10:g.61638140_61638144del, NC_000011.10:g.61638141_61638144del, NC_000011.10:g.61638142_61638144del, NC_000011.10:g.61638143_61638144del, NC_000011.10:g.61638144del, NC_000011.10:g.61638144dup, NC_000011.10:g.61638143_61638144dup, NC_000011.10:g.61638142_61638144dup, NC_000011.10:g.61638141_61638144dup, NC_000011.10:g.61638140_61638144dup, NC_000011.10:g.61638139_61638144dup, NC_000011.10:g.61638138_61638144dup, NC_000011.10:g.61638137_61638144dup, NC_000011.10:g.61638135_61638144dup, NC_000011.10:g.61638134_61638144dup, NC_000011.10:g.61638133_61638144dup, NC_000011.10:g.61638132_61638144dup, NC_000011.10:g.61638131_61638144dup, NC_000011.10:g.61638130_61638144dup, NC_000011.10:g.61638129_61638144dup, NC_000011.10:g.61638128_61638144dup, NC_000011.10:g.61638144_61638145insAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.61638144_61638145insAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.61638144_61638145insAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.61638144_61638145insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.61638144_61638145insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.61405604_61405616del, NC_000011.9:g.61405608_61405616del, NC_000011.9:g.61405609_61405616del, NC_000011.9:g.61405610_61405616del, NC_000011.9:g.61405611_61405616del, NC_000011.9:g.61405612_61405616del, NC_000011.9:g.61405613_61405616del, NC_000011.9:g.61405614_61405616del, NC_000011.9:g.61405615_61405616del, NC_000011.9:g.61405616del, NC_000011.9:g.61405616dup, NC_000011.9:g.61405615_61405616dup, NC_000011.9:g.61405614_61405616dup, NC_000011.9:g.61405613_61405616dup, NC_000011.9:g.61405612_61405616dup, NC_000011.9:g.61405611_61405616dup, NC_000011.9:g.61405610_61405616dup, NC_000011.9:g.61405609_61405616dup, NC_000011.9:g.61405607_61405616dup, NC_000011.9:g.61405606_61405616dup, NC_000011.9:g.61405605_61405616dup, NC_000011.9:g.61405604_61405616dup, NC_000011.9:g.61405603_61405616dup, NC_000011.9:g.61405602_61405616dup, NC_000011.9:g.61405601_61405616dup, NC_000011.9:g.61405600_61405616dup, NC_000011.9:g.61405616_61405617insAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.61405616_61405617insAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.61405616_61405617insAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.61405616_61405617insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.61405616_61405617insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_002775.2:n.2208_2220del, NR_002775.2:n.2212_2220del, NR_002775.2:n.2213_2220del, NR_002775.2:n.2214_2220del, NR_002775.2:n.2215_2220del, NR_002775.2:n.2216_2220del, NR_002775.2:n.2217_2220del, NR_002775.2:n.2218_2220del, NR_002775.2:n.2219_2220del, NR_002775.2:n.2220del, NR_002775.2:n.2220dup, NR_002775.2:n.2219_2220dup, NR_002775.2:n.2218_2220dup, NR_002775.2:n.2217_2220dup, NR_002775.2:n.2216_2220dup, NR_002775.2:n.2215_2220dup, NR_002775.2:n.2214_2220dup, NR_002775.2:n.2213_2220dup, NR_002775.2:n.2211_2220dup, NR_002775.2:n.2210_2220dup, NR_002775.2:n.2209_2220dup, NR_002775.2:n.2208_2220dup, NR_002775.2:n.2207_2220dup, NR_002775.2:n.2206_2220dup, NR_002775.2:n.2205_2220dup, NR_002775.2:n.2204_2220dup, NR_002775.2:n.2220_2221insAAAAAAAAAAAAAAAAAAA, NR_002775.2:n.2220_2221insAAAAAAAAAAAAAAAAAAAA, NR_002775.2:n.2220_2221insAAAAAAAAAAAAAAAAAAAAAAA, NR_002775.2:n.2220_2221insAAAAAAAAAAAAAAAAAAAAAAAAA, NR_002775.2:n.2220_2221insAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 147720766118.

rs1477207661 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 11:61637834 (GRCh38)
11:61405306 (GRCh37)
Canonical SPDI:: NC_000011.10:61637833:AAAA:AAA
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.61637837del, NC_000011.9:g.61405309del, NR_002775.2:n.1913del

Select item 147639881019.

rs1476398810 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:61638992 (GRCh38)
11:61406464 (GRCh37)
Canonical SPDI:: NC_000011.10:61638991:G:A
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.61638992G>A, NC_000011.9:g.61406464G>A, NR_002775.2:n.3068G>A

Select item 147573290120.

rs1475732901 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:61638260 (GRCh38)
11:61405732 (GRCh37)
Canonical SPDI:: NC_000011.10:61638259:G:C
Gene:: RPLP0P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000021/3 (GnomAD)
C=0.00003/8 (TOPMED)
HGVS:: NC_000011.10:g.61638260G>C, NC_000011.9:g.61405732G>C, NR_002775.2:n.2336G>C

<< First< Prev

Page of 52

Next >Last >>

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 1030

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity