SNP Links for Nucleotide (Select 224586781) - SNP

Links from Nucleotide

Items: 1 to 20 of 255

<< First< Prev

Page of 13

Next >Last >>

Select item 14907589161.

rs1490758916 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:41215818 (GRCh38)
6:41183556 (GRCh37)
Canonical SPDI:: NC_000006.12:41215817:A:G
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000091/24 (TOPMED)
G=0.000121/17 (GnomAD)
HGVS:: NC_000006.12:g.41215818A>G, NC_000006.11:g.41183556A>G, NR_027256.1:n.348T>C

Select item 14823799652.

rs1482379965 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:41209092 (GRCh38)
6:41176830 (GRCh37)
Canonical SPDI:: NC_000006.12:41209091:T:G
Gene:: TREML3P (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_000006.12:g.41209092T>G, NC_000006.11:g.41176830T>G, NR_027256.1:n.599A>C

Select item 14751234353.

rs1475123435 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:41209067 (GRCh38)
6:41176805 (GRCh37)
Canonical SPDI:: NC_000006.12:41209066:C:A
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.41209067C>A, NC_000006.11:g.41176805C>A, NR_027256.1:n.624G>T

Select item 14737015954.

rs1473701595 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:41208739 (GRCh38)
6:41176477 (GRCh37)
Canonical SPDI:: NC_000006.12:41208738:G:A
Gene:: TREML3P (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)
HGVS:: NC_000006.12:g.41208739G>A, NC_000006.11:g.41176477G>A, NR_027256.1:n.952C>T

Select item 14734876045.

rs1473487604 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:41208615 (GRCh38)
6:41176353 (GRCh37)
Canonical SPDI:: NC_000006.12:41208614:G:A
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.41208615G>A, NC_000006.11:g.41176353G>A, NR_027256.1:n.1076C>T

Select item 14681193506.

rs1468119350 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:41215807 (GRCh38)
6:41183545 (GRCh37)
Canonical SPDI:: NC_000006.12:41215806:T:A
Gene:: TREML3P (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_000006.12:g.41215807T>A, NC_000006.11:g.41183545T>A, NR_027256.1:n.359A>T

Select item 14632543367.

rs1463254336 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:41208860 (GRCh38)
6:41176598 (GRCh37)
Canonical SPDI:: NC_000006.12:41208859:C:G
Gene:: TREML3P (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=0.000034/9 (TOPMED)
HGVS:: NC_000006.12:g.41208860C>G, NC_000006.11:g.41176598C>G, NR_027256.1:n.831G>C

Select item 14594893228.

rs1459489322 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:41217860 (GRCh38)
6:41185598 (GRCh37)
Canonical SPDI:: NC_000006.12:41217859:G:A
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.41217860G>A, NC_000006.11:g.41185598G>A, NR_027256.1:n.88C>T

Select item 14590287249.

rs1459028724 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:41209152 (GRCh38)
6:41176890 (GRCh37)
Canonical SPDI:: NC_000006.12:41209151:G:A
Gene:: TREML3P (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_000006.12:g.41209152G>A, NC_000006.11:g.41176890G>A, NR_027256.1:n.539C>T

Select item 145790821310.

rs1457908213 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:41217871 (GRCh38)
6:41185609 (GRCh37)
Canonical SPDI:: NC_000006.12:41217870:G:A
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.41217871G>A, NC_000006.11:g.41185609G>A, NR_027256.1:n.77C>T

Select item 145780924011.

rs1457809240 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 6:41217135 (GRCh38)
6:41184873 (GRCh37)
Canonical SPDI:: NC_000006.12:41217134:G:C,NC_000006.12:41217134:G:T
Gene:: TREML3P (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_000006.12:g.41217135G>C, NC_000006.12:g.41217135G>T, NC_000006.11:g.41184873G>C, NC_000006.11:g.41184873G>T, NR_027256.1:n.338C>G, NR_027256.1:n.338C>A

Select item 145173318512.

rs1451733185 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:41209609 (GRCh38)
6:41177347 (GRCh37)
Canonical SPDI:: NC_000006.12:41209608:T:G
Gene:: TREML3P (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_000006.12:g.41209609T>G, NC_000006.11:g.41177347T>G, NR_027256.1:n.526A>C

Select item 145150431913.

rs1451504319 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:41208877 (GRCh38)
6:41176615 (GRCh37)
Canonical SPDI:: NC_000006.12:41208876:C:T
Gene:: TREML3P (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_000006.12:g.41208877C>T, NC_000006.11:g.41176615C>T, NR_027256.1:n.814G>A

Select item 145059863814.

rs1450598638 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:41208778 (GRCh38)
6:41176516 (GRCh37)
Canonical SPDI:: NC_000006.12:41208777:G:T
Gene:: TREML3P (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_000006.12:g.41208778G>T, NC_000006.11:g.41176516G>T, NR_027256.1:n.913C>A

Select item 144904918615.

rs1449049186 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:41208918 (GRCh38)
6:41176656 (GRCh37)
Canonical SPDI:: NC_000006.12:41208917:G:A
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.00003/8 (TOPMED)
HGVS:: NC_000006.12:g.41208918G>A, NC_000006.11:g.41176656G>A, NR_027256.1:n.773C>T

Select item 144039966116.

rs1440399661 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:41208871 (GRCh38)
6:41176609 (GRCh37)
Canonical SPDI:: NC_000006.12:41208870:G:T
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.41208871G>T, NC_000006.11:g.41176609G>T, NR_027256.1:n.820C>A

Select item 143743266117.

rs1437432661 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:41208901 (GRCh38)
6:41176639 (GRCh37)
Canonical SPDI:: NC_000006.12:41208900:G:A
Gene:: TREML3P (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_000006.12:g.41208901G>A, NC_000006.11:g.41176639G>A, NR_027256.1:n.790C>T

Select item 142678690718.

rs1426786907 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:41217686 (GRCh38)
6:41185424 (GRCh37)
Canonical SPDI:: NC_000006.12:41217685:C:T
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.41217686C>T, NC_000006.11:g.41185424C>T, NR_027256.1:n.262G>A

Select item 142566683519.

rs1425666835 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 6:41217758 (GRCh38)
6:41185496 (GRCh37)
Canonical SPDI:: NC_000006.12:41217757:T:A,NC_000006.12:41217757:T:C
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000006.12:g.41217758T>A, NC_000006.12:g.41217758T>C, NC_000006.11:g.41185496T>A, NC_000006.11:g.41185496T>C, NR_027256.1:n.190A>T, NR_027256.1:n.190A>G

Select item 142558801520.

rs1425588015 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:41215769 (GRCh38)
6:41183507 (GRCh37)
Canonical SPDI:: NC_000006.12:41215768:C:A,NC_000006.12:41215768:C:T
Gene:: TREML3P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.41215769C>A, NC_000006.12:g.41215769C>T, NC_000006.11:g.41183507C>A, NC_000006.11:g.41183507C>T, NR_027256.1:n.397G>T, NR_027256.1:n.397G>A

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 255

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity