SNP Links for Nucleotide (Select 256017203) - SNP

Links from Nucleotide

Items: 1 to 20 of 194

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Select item 14900591171.

rs1490059117 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:22299725 (GRCh38)
17:21826331 (GRCh37)
Canonical SPDI:: NC_000017.11:22299724:A:G
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000017.11:g.22299725A>G, NC_000017.10:g.21826331A>G, NR_028336.1:n.441A>G, NM_203392.1:c.*31A>G

Select item 14895208302.

rs1489520830 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:22299712 (GRCh38)
17:21826318 (GRCh37)
Canonical SPDI:: NC_000017.11:22299711:C:T
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000084/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.22299712C>T, NC_000017.10:g.21826318C>T, NR_028336.1:n.428C>T, NM_203392.1:c.*18C>T

Select item 14849576413.

rs1484957641 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 17:22299674 (GRCh38)
17:21826280 (GRCh37)
Canonical SPDI:: NC_000017.11:22299673:CT:
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.22299674_22299675del, NC_000017.10:g.21826280_21826281del, NR_028336.1:n.390_391del, NM_203392.1:c.196_197del

Select item 14830575374.

rs1483057537 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 17:22299563 (GRCh38)
17:21826169 (GRCh37)
Canonical SPDI:: NC_000017.11:22299562:CCC:CC
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000017.11:g.22299565del, NC_000017.10:g.21826171del, NR_028336.1:n.281del, NM_203392.1:c.87del

Select item 14810583015.

rs1481058301 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:22298960 (GRCh38)
17:21825566 (GRCh37)
Canonical SPDI:: NC_000017.11:22298959:G:A
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.22298960G>A, NC_000017.10:g.21825566G>A, NR_028336.1:n.197G>A, NM_203392.1:c.3G>A

Select item 14710739076.

rs1471073907 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:22299612 (GRCh38)
17:21826218 (GRCh37)
Canonical SPDI:: NC_000017.11:22299611:G:A
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.22299612G>A, NC_000017.10:g.21826218G>A, NR_028336.1:n.328G>A, NM_203392.1:c.134G>A

Select item 14704867267.

rs1470486726 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:22298917 (GRCh38)
17:21825523 (GRCh37)
Canonical SPDI:: NC_000017.11:22298916:C:T
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.22298917C>T, NC_000017.10:g.21825523C>T, NR_028336.1:n.154C>T, NM_203392.1:c.-41C>T

Select item 14702524698.

rs1470252469 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:22299577 (GRCh38)
17:21826183 (GRCh37)
Canonical SPDI:: NC_000017.11:22299576:G:A,NC_000017.11:22299576:G:T
Gene:: FAM27E5 (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_000017.11:g.22299577G>A, NC_000017.11:g.22299577G>T, NC_000017.10:g.21826183G>A, NC_000017.10:g.21826183G>T, NR_028336.1:n.293G>A, NR_028336.1:n.293G>T, NM_203392.1:c.99G>A, NM_203392.1:c.99G>T

Select item 14623901039.

rs1462390103 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 17:22299562 (GRCh38)
17:21826168 (GRCh37)
Canonical SPDI:: NC_000017.11:22299561:G:A,NC_000017.11:22299561:G:C
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.22299562G>A, NC_000017.11:g.22299562G>C, NC_000017.10:g.21826168G>A, NC_000017.10:g.21826168G>C, NR_028336.1:n.278G>A, NR_028336.1:n.278G>C, NM_203392.1:c.84G>A, NM_203392.1:c.84G>C

Select item 146156484610.

rs1461564846 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:22299759 (GRCh38)
17:21826365 (GRCh37)
Canonical SPDI:: NC_000017.11:22299758:C:T
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000017.11:g.22299759C>T, NC_000017.10:g.21826365C>T, NR_028336.1:n.475C>T, NM_203392.1:c.*65C>T

Select item 145580588711.

rs1455805887 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:22298854 (GRCh38)
17:21825460 (GRCh37)
Canonical SPDI:: NC_000017.11:22298853:G:A
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000017.11:g.22298854G>A, NC_000017.10:g.21825460G>A, NR_028336.1:n.91G>A, NM_203392.1:c.-104G>A

Select item 144993989612.

rs1449939896 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 17:22299623 (GRCh38)
17:21826229 (GRCh37)
Canonical SPDI:: NC_000017.11:22299622:C:A,NC_000017.11:22299622:C:T
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.22299623C>A, NC_000017.11:g.22299623C>T, NC_000017.10:g.21826229C>A, NC_000017.10:g.21826229C>T, NR_028336.1:n.339C>A, NR_028336.1:n.339C>T, NM_203392.1:c.145C>A, NM_203392.1:c.145C>T

Select item 144965540813.

rs1449655408 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 17:22299627 (GRCh38)
17:21826233 (GRCh37)
Canonical SPDI:: NC_000017.11:22299626:G:A,NC_000017.11:22299626:G:C
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000023/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.22299627G>A, NC_000017.11:g.22299627G>C, NC_000017.10:g.21826233G>A, NC_000017.10:g.21826233G>C, NR_028336.1:n.343G>A, NR_028336.1:n.343G>C, NM_203392.1:c.149G>A, NM_203392.1:c.149G>C

Select item 144588197314.

rs1445881973 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 17:22299501 (GRCh38)
17:21826107 (GRCh37)
Canonical SPDI:: NC_000017.11:22299500:C:A
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.22299501C>A, NC_000017.10:g.21826107C>A, NR_028336.1:n.217C>A, NM_203392.1:c.23C>A

Select item 143113346515.

rs1431133465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:22299676 (GRCh38)
17:21826282 (GRCh37)
Canonical SPDI:: NC_000017.11:22299675:G:C
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.22299676G>C, NC_000017.10:g.21826282G>C, NR_028336.1:n.392G>C, NM_203392.1:c.198G>C

Select item 142901186116.

rs1429011861 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:22299560 (GRCh38)
17:21826166 (GRCh37)
Canonical SPDI:: NC_000017.11:22299559:A:G
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.22299560A>G, NC_000017.10:g.21826166A>G, NR_028336.1:n.276A>G, NM_203392.1:c.82A>G

Select item 142796471217.

rs1427964712 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:22298844 (GRCh38)
17:21825450 (GRCh37)
Canonical SPDI:: NC_000017.11:22298843:G:A
Gene:: FAM27E5 (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_000017.11:g.22298844G>A, NC_000017.10:g.21825450G>A, NR_028336.1:n.81G>A, NM_203392.1:c.-114G>A

Select item 142346038718.

rs1423460387 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:22299655 (GRCh38)
17:21826261 (GRCh37)
Canonical SPDI:: NC_000017.11:22299654:T:C
Gene:: FAM27E5 (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_000017.11:g.22299655T>C, NC_000017.10:g.21826261T>C, NR_028336.1:n.371T>C, NM_203392.1:c.177T>C

Select item 142301143019.

rs1423011430 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:22299579 (GRCh38)
17:21826185 (GRCh37)
Canonical SPDI:: NC_000017.11:22299578:T:C
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000017.11:g.22299579T>C, NC_000017.10:g.21826185T>C, NR_028336.1:n.295T>C, NM_203392.1:c.101T>C

Select item 142086518620.

rs1420865186 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:22299643 (GRCh38)
17:21826249 (GRCh37)
Canonical SPDI:: NC_000017.11:22299642:G:T
Gene:: FAM27E5 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.22299643G>T, NC_000017.10:g.21826249G>T, NR_028336.1:n.359G>T, NM_203392.1:c.165G>T

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Links from Nucleotide

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