SNP Links for Nucleotide (Select 608601834) - SNP

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Links from Nucleotide

Items: 1 to 20 of 612

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Select item 14914190551.

rs1491419055 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 9:39445214 (GRCh38)
9:39445213 (GRCh37)
Canonical SPDI:: NC_000009.12:39445213:CT:
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000142/2 (ALFA)
-=0.000071/10 (GnomAD)
-=0.000094/25 (TOPMED)
HGVS:: NC_000009.12:g.39445214_39445215del, NC_000009.11:g.39445213_39445214del, NR_003528.3:n.2628_2629del, NR_003528.2:n.2628_2629del, NM_001032297.1:c.1743_1744del, NR_027861.1:n.1975_1976del

Select item 14911214042.

rs1491121404 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TG [Show Flanks]
Chromosome:: 9:39445214 (GRCh38)
9:39445214 (GRCh37)
Canonical SPDI:: NC_000009.12:39445214:TGTGTG:TGTGTGTG
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTG=0./0 (ALFA)
TG=0.000007/1 (GnomAD)
TG=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.39445215TG[4], NC_000009.11:g.39445214TG[4], NR_003528.3:n.2623CA[4], NR_003528.2:n.2623CA[4], NM_001032297.1:c.1742_1743dup, NR_027861.1:n.1970CA[4]

Select item 14884422003.

rs1488442200 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:39464432 (GRCh38)
9:41609450 (GRCh37)
Canonical SPDI:: NC_000009.12:39464431:C:A
Gene:: ZNF658B (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=0.000008/2 (TOPMED)
A=0.000546/1 (Korea1K)
HGVS:: NC_000009.12:g.39464432C>A, NC_000009.11:g.41609450C>A, NR_003528.3:n.95G>T, NR_003528.2:n.95G>T

Select item 14881520834.

rs1488152083 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:39445639 (GRCh38)
9:39445638 (GRCh37)
Canonical SPDI:: NC_000009.12:39445638:T:C
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000156/1 (1000Genomes)
HGVS:: NC_000009.12:g.39445639T>C, NC_000009.11:g.39445638T>C, NR_003528.3:n.2204A>G, NR_003528.2:n.2204A>G, NM_001032297.1:c.1319A>G, NR_027861.1:n.1551A>G

Select item 14871344465.

rs1487134446 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:39444756 (GRCh38)
9:39444755 (GRCh37)
Canonical SPDI:: NC_000009.12:39444755:C:A,NC_000009.12:39444755:C:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.39444756C>A, NC_000009.12:g.39444756C>T, NC_000009.11:g.39444755C>A, NC_000009.11:g.39444755C>T, NR_003528.3:n.3087G>T, NR_003528.3:n.3087G>A, NR_003528.2:n.3087G>T, NR_003528.2:n.3087G>A, NM_001032297.1:c.2202G>T, NM_001032297.1:c.2202G>A, NR_027861.1:n.2434G>T, NR_027861.1:n.2434G>A

Select item 14870778046.

rs1487077804 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:39456582 (GRCh38)
9:41601600 (GRCh37)
Canonical SPDI:: NC_000009.12:39456581:C:A,NC_000009.12:39456581:C:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.39456582C>A, NC_000009.12:g.39456582C>T, NC_000009.11:g.41601600C>A, NC_000009.11:g.41601600C>T, NR_003528.3:n.317G>T, NR_003528.3:n.317G>A, NR_003528.2:n.317G>T, NR_003528.2:n.317G>A

Select item 14870724897.

rs1487072489 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 9:39445215 (GRCh38)
9:39445214 (GRCh37)
Canonical SPDI:: NC_000009.12:39445214:T:
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.39445215del, NC_000009.11:g.39445214del, NR_003528.3:n.2628del, NR_003528.2:n.2628del, NM_001032297.1:c.1743del, NR_027861.1:n.1975del

Select item 14865008368.

rs1486500836 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:39446451 (GRCh38)
9:41591469 (GRCh37)
Canonical SPDI:: NC_000009.12:39446450:C:G
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000057/15 (TOPMED)
HGVS:: NC_000009.12:g.39446451C>G, NC_000009.11:g.41591469C>G, NR_003528.3:n.1392G>C, NR_003528.2:n.1392G>C, NM_001032297.1:c.507G>C, NR_027861.1:n.739G>C

Select item 14864812279.

rs1486481227 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:39445545 (GRCh38)
9:39445544 (GRCh37)
Canonical SPDI:: NC_000009.12:39445544:C:A
Gene:: ZNF658B (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.39445545C>A, NC_000009.11:g.39445544C>A, NR_003528.3:n.2298G>T, NR_003528.2:n.2298G>T, NM_001032297.1:c.1413G>T, NR_027861.1:n.1645G>T

Select item 148615360710.

rs1486153607 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:39445125 (GRCh38)
9:39445124 (GRCh37)
Canonical SPDI:: NC_000009.12:39445124:T:C
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000337/4 (ALFA)
C=0.000189/26 (GnomAD)
C=0.000625/4 (1000Genomes)
HGVS:: NC_000009.12:g.39445125T>C, NC_000009.11:g.39445124T>C, NR_003528.3:n.2718A>G, NR_003528.2:n.2718A>G, NM_001032297.1:c.1833A>G, NR_027861.1:n.2065A>G

Select item 148610139511.

rs1486101395 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:39446094 (GRCh38)
9:41591112 (GRCh37)
Canonical SPDI:: NC_000009.12:39446093:G:C
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.39446094G>C, NC_000009.11:g.41591112G>C, NR_003528.3:n.1749C>G, NR_003528.2:n.1749C>G, NM_001032297.1:c.864C>G, NR_027861.1:n.1096C>G

Select item 148571393012.

rs1485713930 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:39461686 (GRCh38)
9:41606704 (GRCh37)
Canonical SPDI:: NC_000009.12:39461685:G:A
Gene:: ZNF658B (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=0.000012/1 (GnomAD)
HGVS:: NC_000009.12:g.39461686G>A, NC_000009.11:g.41606704G>A, NR_003528.3:n.158C>T, NR_003528.2:n.158C>T

Select item 148552205713.

rs1485522057 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:39446840 (GRCh38)
9:41591858 (GRCh37)
Canonical SPDI:: NC_000009.12:39446839:C:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.006263/88 (ALFA)
T=0.000546/1 (Korea1K)
T=0.000814/23 (TOMMO)
T=0.008288/1160 (GnomAD)
T=0.008588/55 (1000Genomes)
T=0.009116/2413 (TOPMED)
HGVS:: NC_000009.12:g.39446840C>T, NC_000009.11:g.41591858C>T, NR_003528.3:n.1003G>A, NR_003528.2:n.1003G>A, NM_001032297.1:c.118G>A, NR_027861.1:n.350G>A

Select item 148550170414.

rs1485501704 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCCCCT>- [Show Flanks]
Chromosome:: 9:39445965 (GRCh38)
9:41590983 (GRCh37)
Canonical SPDI:: NC_000009.12:39445963:TCTCCCCT:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.39445965_39445971del, NC_000009.11:g.41590983_41590989del, NR_003528.3:n.1873_1879del, NR_003528.2:n.1873_1879del, NM_001032297.1:c.988_994del, NR_027861.1:n.1220_1226del

Select item 148489133215.

rs1484891332 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:39446532 (GRCh38)
9:41591550 (GRCh37)
Canonical SPDI:: NC_000009.12:39446531:A:G
Gene:: ZNF658B (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.39446532A>G, NC_000009.11:g.41591550A>G, NR_003528.3:n.1311T>C, NR_003528.2:n.1311T>C, NM_001032297.1:c.426T>C, NR_027861.1:n.658T>C

Select item 148423502616.

rs1484235026 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:39447371 (GRCh38)
9:41592389 (GRCh37)
Canonical SPDI:: NC_000009.12:39447370:G:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.39447371G>T, NC_000009.11:g.41592389G>T, NR_003528.3:n.472C>A, NR_003528.2:n.472C>A

Select item 148324576517.

rs1483245765 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:39447284 (GRCh38)
9:41592302 (GRCh37)
Canonical SPDI:: NC_000009.12:39447283:G:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000107/15 (GnomAD)
T=0.000121/32 (TOPMED)
HGVS:: NC_000009.12:g.39447284G>T, NC_000009.11:g.41592302G>T, NR_003528.3:n.559C>A, NR_003528.2:n.559C>A

Select item 148079116418.

rs1480791164 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:39446442 (GRCh38)
9:41591460 (GRCh37)
Canonical SPDI:: NC_000009.12:39446441:G:A,NC_000009.12:39446441:G:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00265/17 (1000Genomes)
HGVS:: NC_000009.12:g.39446442G>A, NC_000009.12:g.39446442G>T, NC_000009.11:g.41591460G>A, NC_000009.11:g.41591460G>T, NR_003528.3:n.1401C>T, NR_003528.3:n.1401C>A, NR_003528.2:n.1401C>T, NR_003528.2:n.1401C>A, NM_001032297.1:c.516C>T, NM_001032297.1:c.516C>A, NR_027861.1:n.748C>T, NR_027861.1:n.748C>A

Select item 148063859419.

rs1480638594 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:39445397 (GRCh38)
9:39445396 (GRCh37)
Canonical SPDI:: NC_000009.12:39445396:G:A,NC_000009.12:39445396:G:T
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000091/24 (TOPMED)
A=0.000312/2 (1000Genomes)
HGVS:: NC_000009.12:g.39445397G>A, NC_000009.12:g.39445397G>T, NC_000009.11:g.39445396G>A, NC_000009.11:g.39445396G>T, NR_003528.3:n.2446C>T, NR_003528.3:n.2446C>A, NR_003528.2:n.2446C>T, NR_003528.2:n.2446C>A, NM_001032297.1:c.1561C>T, NM_001032297.1:c.1561C>A, NR_027861.1:n.1793C>T, NR_027861.1:n.1793C>A

Select item 148010747720.

rs1480107477 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:39447280 (GRCh38)
9:41592298 (GRCh37)
Canonical SPDI:: NC_000009.12:39447279:A:G
Gene:: ZNF658B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000021/3 (GnomAD)
G=0.000034/9 (TOPMED)
HGVS:: NC_000009.12:g.39447280A>G, NC_000009.11:g.41592298A>G, NR_003528.3:n.563T>C, NR_003528.2:n.563T>C