SNP Links for Nucleotide (Select 652699963) - SNP

Links from Nucleotide

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Select item 14898380631.

rs1489838063 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 9:126270165 (GRCh38)
9:129032445 (GRCh37)
Canonical SPDI:: NC_000009.12:126270165:A:AA
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0.000142/2 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.126270166dup, NC_000009.11:g.129032445dup, NR_121584.1:n.2054dup

Select item 14892806012.

rs1489280601 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:126271707 (GRCh38)
9:129033986 (GRCh37)
Canonical SPDI:: NC_000009.12:126271706:A:G
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.126271707A>G, NC_000009.11:g.129033986A>G, NR_121584.1:n.513T>C

Select item 14891782943.

rs1489178294 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:126270181 (GRCh38)
9:129032460 (GRCh37)
Canonical SPDI:: NC_000009.12:126270180:T:C
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.126270181T>C, NC_000009.11:g.129032460T>C, NR_121584.1:n.2039A>G

Select item 14888166324.

rs1488816632 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:126270486 (GRCh38)
9:129032765 (GRCh37)
Canonical SPDI:: NC_000009.12:126270485:G:A
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.126270486G>A, NC_000009.11:g.129032765G>A, NR_121584.1:n.1734C>T

Select item 14883011065.

rs1488301106 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:126271145 (GRCh38)
9:129033424 (GRCh37)
Canonical SPDI:: NC_000009.12:126271144:A:G
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.126271145A>G, NC_000009.11:g.129033424A>G, NR_121584.1:n.1075T>C

Select item 14814787766.

rs1481478776 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:126275850 (GRCh38)
9:129038129 (GRCh37)
Canonical SPDI:: NC_000009.12:126275849:C:G
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000009.12:g.126275850C>G, NC_000009.11:g.129038129C>G, NR_121584.1:n.66G>C

Select item 14801580907.

rs1480158090 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:126271554 (GRCh38)
9:129033833 (GRCh37)
Canonical SPDI:: NC_000009.12:126271553:A:G
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.126271554A>G, NC_000009.11:g.129033833A>G, NR_121584.1:n.666T>C

Select item 14753849858.

rs1475384985 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 9:126271795 (GRCh38)
9:129034074 (GRCh37)
Canonical SPDI:: NC_000009.12:126271794:T:A,NC_000009.12:126271794:T:G
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.126271795T>A, NC_000009.12:g.126271795T>G, NC_000009.11:g.129034074T>A, NC_000009.11:g.129034074T>G, NR_121584.1:n.425A>T, NR_121584.1:n.425A>C

Select item 14743758289.

rs1474375828 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 9:126270845 (GRCh38)
9:129033124 (GRCh37)
Canonical SPDI:: NC_000009.12:126270844:T:C,NC_000009.12:126270844:T:G
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000342/1 (KOREAN)
HGVS:: NC_000009.12:g.126270845T>C, NC_000009.12:g.126270845T>G, NC_000009.11:g.129033124T>C, NC_000009.11:g.129033124T>G, NR_121584.1:n.1375A>G, NR_121584.1:n.1375A>C

Select item 147420323010.

rs1474203230 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:126271851 (GRCh38)
9:129034130 (GRCh37)
Canonical SPDI:: NC_000009.12:126271850:C:T
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.126271851C>T, NC_000009.11:g.129034130C>T, NR_121584.1:n.369G>A

Select item 147259855711.

rs1472598557 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:126271157 (GRCh38)
9:129033436 (GRCh37)
Canonical SPDI:: NC_000009.12:126271156:C:T
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00003/8 (TOPMED)
T=0.000036/5 (GnomAD)
T=0.000106/2 (TOMMO)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000009.12:g.126271157C>T, NC_000009.11:g.129033436C>T, NR_121584.1:n.1063G>A

Select item 146703769212.

rs1467037692 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:126270446 (GRCh38)
9:129032725 (GRCh37)
Canonical SPDI:: NC_000009.12:126270445:T:C
Gene:: LOC101929116 (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=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.126270446T>C, NC_000009.11:g.129032725T>C, NR_121584.1:n.1774A>G

Select item 146702266713.

rs1467022667 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:126271380 (GRCh38)
9:129033659 (GRCh37)
Canonical SPDI:: NC_000009.12:126271379:C:G,NC_000009.12:126271379:C:T
Gene:: LOC101929116 (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_000009.12:g.126271380C>G, NC_000009.12:g.126271380C>T, NC_000009.11:g.129033659C>G, NC_000009.11:g.129033659C>T, NR_121584.1:n.840G>C, NR_121584.1:n.840G>A

Select item 146644012714.

rs1466440127 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:126270778 (GRCh38)
9:129033057 (GRCh37)
Canonical SPDI:: NC_000009.12:126270777:G:A
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.126270778G>A, NC_000009.11:g.129033057G>A, NR_121584.1:n.1442C>T

Select item 146544734115.

rs1465447341 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:126270286 (GRCh38)
9:129032565 (GRCh37)
Canonical SPDI:: NC_000009.12:126270285:C:T
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.126270286C>T, NC_000009.11:g.129032565C>T, NR_121584.1:n.1934G>A

Select item 146177451016.

rs1461774510 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:126271875 (GRCh38)
9:129034154 (GRCh37)
Canonical SPDI:: NC_000009.12:126271874:T:C
Gene:: LOC101929116 (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)
C=0.000035/1 (TOMMO)
HGVS:: NC_000009.12:g.126271875T>C, NC_000009.11:g.129034154T>C, NR_121584.1:n.345A>G

Select item 146176275617.

rs1461762756 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:126271500 (GRCh38)
9:129033779 (GRCh37)
Canonical SPDI:: NC_000009.12:126271499:A:G
Gene:: LOC101929116 (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_000009.12:g.126271500A>G, NC_000009.11:g.129033779A>G, NR_121584.1:n.720T>C

Select item 146014647418.

rs1460146474 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAAAATATAATATAAATAAAATAAAATAAAATAAA [Show Flanks]
Chromosome:: 9:126271073 (GRCh38)
9:129033353 (GRCh37)
Canonical SPDI:: NC_000009.12:126271073:AAA:AAATAAAATATAATATAAATAAAATAAAATAAAATAAA
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AAATAAAATATAATATAAATAAAATAAAATAAAATAAA=0.0002/1 (ALFA)
HGVS:: NC_000009.12:g.126271074_126271076AAATA[2]TAATATAAATAAAATAAAATAAAATAAA[1], NC_000009.11:g.129033353_129033355AAATA[2]TAATATAAATAAAATAAAATAAAATAAA[1], NR_121584.1:n.1144_1146TTTAT[4]TTATA[2]T[4]ATTT[1]

Select item 145746780819.

rs1457467808 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:126270859 (GRCh38)
9:129033138 (GRCh37)
Canonical SPDI:: NC_000009.12:126270858:C:A
Gene:: LOC101929116 (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_000009.12:g.126270859C>A, NC_000009.11:g.129033138C>A, NR_121584.1:n.1361G>T

Select item 145278140420.

rs1452781404 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:126271827 (GRCh38)
9:129034106 (GRCh37)
Canonical SPDI:: NC_000009.12:126271826:G:A
Gene:: LOC101929116 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000029/4 (GnomAD)
A=0.000312/2 (1000Genomes)
HGVS:: NC_000009.12:g.126271827G>A, NC_000009.11:g.129034106G>A, NR_121584.1:n.393C>T

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