SNP Links for Nucleotide (Select 586946409) - SNP

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Links from Nucleotide

Items: 1 to 20 of 633

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Select item 14895230191.

rs1489523019 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161600511 (GRCh38)
1:161570301 (GRCh37)
Canonical SPDI:: NC_000001.11:161600510:C:T
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000169/2 (ALFA)
T=0./0 (KOREAN)
T=0.000097/13 (GnomAD)
HGVS:: NC_000001.11:g.161600511C>T, NC_000001.10:g.161570301C>T, NG_011982.1:g.24173C>T, NM_201563.5:c.*708C>T, NR_047648.1:n.1779C>T

Select item 14889182022.

rs1488918202 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:161589786 (GRCh38)
1:161559576 (GRCh37)
Canonical SPDI:: NC_000001.11:161589785:C:A
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161589786C>A, NC_000001.10:g.161559576C>A, NG_011982.1:g.13448C>A, NM_201563.5:c.358C>A, NM_201563.4:c.358C>A, NR_047648.1:n.457C>A, NM_001005410.2:c.358C>A, NM_001005412.1:c.358C>A

Select item 14858492293.

rs1485849229 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:161600192 (GRCh38)
1:161569982 (GRCh37)
Canonical SPDI:: NC_000001.11:161600191:T:A
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000001.11:g.161600192T>A, NC_000001.10:g.161569982T>A, NG_011982.1:g.23854T>A, NM_201563.5:c.*389T>A, NM_201563.4:c.*389T>A, NR_047648.1:n.1460T>A, NM_001005410.2:c.*544T>A

Select item 14856328714.

rs1485632871 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:161601184 (GRCh38)
1:161570974 (GRCh37)
Canonical SPDI:: NC_000001.11:161601183:A:G
Gene:: FCGR2C (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=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.161601184A>G, NC_000001.10:g.161570974A>G, NG_011982.1:g.24846A>G, NM_201563.5:c.*1381A>G, NR_047648.1:n.2452A>G

Select item 14833576785.

rs1483357678 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:161591270 (GRCh38)
1:161561060 (GRCh37)
Canonical SPDI:: NC_000001.11:161591269:A:C
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.161591270A>C, NC_000001.10:g.161561060A>C, NG_011982.1:g.14932A>C, NM_201563.5:c.518A>C, NM_201563.4:c.518A>C, NR_047648.1:n.617A>C, NM_001005410.2:c.518A>C, NM_001005412.1:c.518A>C

Select item 14816774916.

rs1481677491 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:161592156 (GRCh38)
1:161561946 (GRCh37)
Canonical SPDI:: NC_000001.11:161592155:T:C
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD_exomes)
C=0.000042/5 (GnomAD)
HGVS:: NC_000001.11:g.161592156T>C, NC_000001.10:g.161561946T>C, NG_011982.1:g.15818T>C, NM_201563.5:c.674T>C, NM_201563.4:c.674T>C, NR_047648.1:n.773T>C, NM_001005410.2:c.674T>C, NM_001005412.1:c.*54T>C

Select item 14815295267.

rs1481529526 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:161600124 (GRCh38)
1:161569914 (GRCh37)
Canonical SPDI:: NC_000001.11:161600123:T:C
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00018/3 (TOMMO)
HGVS:: NC_000001.11:g.161600124T>C, NC_000001.10:g.161569914T>C, NG_011982.1:g.23786T>C, NM_201563.5:c.*321T>C, NM_201563.4:c.*321T>C, NR_047648.1:n.1392T>C, NM_001005410.2:c.*476T>C

Select item 14806508908.

rs1480650890 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:161600584 (GRCh38)
1:161570374 (GRCh37)
Canonical SPDI:: NC_000001.11:161600583:C:A
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/2 (GnomAD)
HGVS:: NC_000001.11:g.161600584C>A, NC_000001.10:g.161570374C>A, NG_011982.1:g.24246C>A, NM_201563.5:c.*781C>A, NR_047648.1:n.1852C>A

Select item 14791028329.

rs1479102832 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:161600419 (GRCh38)
1:161570209 (GRCh37)
Canonical SPDI:: NC_000001.11:161600418:A:C
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000422/5 (ALFA)
C=0.000178/24 (GnomAD)
HGVS:: NC_000001.11:g.161600419A>C, NC_000001.10:g.161570209A>C, NG_011982.1:g.24081A>C, NM_201563.5:c.*616A>C, NR_047648.1:n.1687A>C

Select item 147748180610.

rs1477481806 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:161600251 (GRCh38)
1:161570041 (GRCh37)
Canonical SPDI:: NC_000001.11:161600250:G:A
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00003/4 (GnomAD)
A=0.000035/1 (TOMMO)
A=0.000343/1 (KOREAN)
A=0.000546/1 (Korea1K)
HGVS:: NC_000001.11:g.161600251G>A, NC_000001.10:g.161570041G>A, NG_011982.1:g.23913G>A, NM_201563.5:c.*448G>A, NR_047648.1:n.1519G>A

Select item 147721218111.

rs1477212181 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:161595579 (GRCh38)
1:161565369 (GRCh37)
Canonical SPDI:: NC_000001.11:161595578:G:A
Gene:: FCGR2C (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_000001.11:g.161595579G>A, NC_000001.10:g.161565369G>A, NG_011982.1:g.19241G>A, NM_201563.5:c.787G>A, NM_201563.4:c.787G>A, NR_047648.1:n.886G>A, NM_001005410.2:c.787G>A

Select item 147677519612.

rs1476775196 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:161591202 (GRCh38)
1:161560992 (GRCh37)
Canonical SPDI:: NC_000001.11:161591201:G:A
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000001.11:g.161591202G>A, NC_000001.10:g.161560992G>A, NG_011982.1:g.14864G>A, NM_201563.5:c.450G>A, NM_201563.4:c.450G>A, NR_047648.1:n.549G>A, NM_001005410.2:c.450G>A, NM_001005412.1:c.450G>A

Select item 147531469513.

rs1475314695 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AG [Show Flanks]
Chromosome:: 1:161600287 (GRCh38)
1:161570078 (GRCh37)
Canonical SPDI:: NC_000001.11:161600287:AG:AGAG
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAG=0.00017/2 (ALFA)
AG=0.00014/2 (TOMMO)
AG=0.00031/2 (1000Genomes)
HGVS:: NC_000001.11:g.161600288_161600289dup, NC_000001.10:g.161570078_161570079dup, NG_011982.1:g.23950_23951dup, NM_201563.5:c.*485_*486dup, NR_047648.1:n.1556_1557dup

Select item 147474059714.

rs1474740597 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:161600868 (GRCh38)
1:161570658 (GRCh37)
Canonical SPDI:: NC_000001.11:161600867:C:A
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000001.11:g.161600868C>A, NC_000001.10:g.161570658C>A, NG_011982.1:g.24530C>A, NM_201563.5:c.*1065C>A, NR_047648.1:n.2136C>A

Select item 147230029915.

rs1472300299 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:161600169 (GRCh38)
1:161569959 (GRCh37)
Canonical SPDI:: NC_000001.11:161600168:G:A,NC_000001.11:161600168:G:T
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.161600169G>A, NC_000001.11:g.161600169G>T, NC_000001.10:g.161569959G>A, NC_000001.10:g.161569959G>T, NG_011982.1:g.23831G>A, NG_011982.1:g.23831G>T, NM_201563.5:c.*366G>A, NM_201563.5:c.*366G>T, NM_201563.4:c.*366G>A, NM_201563.4:c.*366G>T, NR_047648.1:n.1437G>A, NR_047648.1:n.1437G>T, NM_001005410.2:c.*521G>A, NM_001005410.2:c.*521G>T

Select item 147109010216.

rs1471090102 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:161601047 (GRCh38)
1:161570837 (GRCh37)
Canonical SPDI:: NC_000001.11:161601046:G:A,NC_000001.11:161601046:G:T
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000546/1 (Korea1K)
HGVS:: NC_000001.11:g.161601047G>A, NC_000001.11:g.161601047G>T, NC_000001.10:g.161570837G>A, NC_000001.10:g.161570837G>T, NG_011982.1:g.24709G>A, NG_011982.1:g.24709G>T, NM_201563.5:c.*1244G>A, NM_201563.5:c.*1244G>T, NR_047648.1:n.2315G>A, NR_047648.1:n.2315G>T

Select item 147008200717.

rs1470082007 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:161599687 (GRCh38)
1:161569477 (GRCh37)
Canonical SPDI:: NC_000001.11:161599686:G:C
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/1 (GnomAD)
HGVS:: NC_000001.11:g.161599687G>C, NC_000001.10:g.161569477G>C, NG_011982.1:g.23349G>C, NM_201563.5:c.856G>C, NM_201563.4:c.856G>C, NR_047648.1:n.955G>C, NM_001005410.2:c.*39G>C, NM_001005412.1:c.*198G>C

Select item 146925962818.

rs1469259628 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161600824 (GRCh38)
1:161570614 (GRCh37)
Canonical SPDI:: NC_000001.11:161600823:C:T
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/2 (GnomAD)
HGVS:: NC_000001.11:g.161600824C>T, NC_000001.10:g.161570614C>T, NG_011982.1:g.24486C>T, NM_201563.5:c.*1021C>T, NR_047648.1:n.2092C>T

Select item 146861818919.

rs1468618189 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:161599701 (GRCh38)
1:161569491 (GRCh37)
Canonical SPDI:: NC_000001.11:161599700:T:C
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161599701T>C, NC_000001.10:g.161569491T>C, NG_011982.1:g.23363T>C, NM_201563.5:c.870T>C, NM_201563.4:c.870T>C, NR_047648.1:n.969T>C, NM_001005410.2:c.*53T>C

Select item 146754931320.

rs1467549313 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:161600235 (GRCh38)
1:161570025 (GRCh37)
Canonical SPDI:: NC_000001.11:161600234:A:G
Gene:: FCGR2C (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.161600235A>G, NC_000001.10:g.161570025A>G, NG_011982.1:g.23897A>G, NM_201563.5:c.*432A>G, NM_201563.4:c.*432A>G, NR_047648.1:n.1503A>G, NM_001005410.2:c.*587A>G

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