SNP Links for Gene (Select 100507395) - SNP

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Links from Gene

Items: 1 to 20 of 132

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Select item 3868302111.

rs386830211 has merged into rs76803014 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: NT_167214.1:9821 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:9821:TTTTTTT:TTTTTTTT
Gene:: LOC100507395 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.9828dup

Select item 3868302102.

rs386830210 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: NT_167214.1:9821 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:9820:A:
Gene:: LOC100507395 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NT_167214.1:g.9821del

Select item 3868302053.

rs386830205 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: NT_167214.1:8646 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:8645:TTTTTTTTTT:TTTTTTTTT
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.8655del, XR_950600.3:n.747del

Select item 3868302034.

rs386830203 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TC [Show Flanks]
Chromosome:: NT_167214.1:8296 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:8296:TCTC:TCTCTC
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.8297TC[3], XR_950600.3:n.1093GA[3], XR_950600.2:n.339GA[3]

Select item 3868301975.

rs386830197 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: NT_167214.1:7970 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:7969:G:C
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.7970G>C, XR_950600.3:n.1423C>G, XR_950600.2:n.669C>G

Select item 3868301896.

rs386830189 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: NT_167214.1:7401 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:7400:C:T
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.7401C>T, XR_950600.3:n.1992G>A, XR_950600.2:n.1238G>A, XR_950600.1:n.131G>A

Select item 3868301877.

rs386830187 has merged into rs74220393 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: NT_167214.1:7385 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:7384:G:C
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.7385G>C, XR_950600.3:n.2008C>G, XR_950600.2:n.1254C>G, XR_950600.1:n.147C>G

Select item 3868301838.

rs386830183 has merged into rs74210180 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: NT_167214.1:7116 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:7115:GG:G
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.7117del, XR_950600.3:n.2277del, XR_950600.2:n.1523del, XR_950600.1:n.416del

Select item 3868301819.

rs386830181 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: NT_167214.1:6910 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:6909:G:T
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.6910G>T, XR_950600.3:n.2483C>A, XR_950600.2:n.1729C>A, XR_950600.1:n.622C>A

Select item 38683018010.

rs386830180 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: NT_167214.1:6908 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:6907:G:A
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.6908G>A, XR_950600.3:n.2485C>T, XR_950600.2:n.1731C>T, XR_950600.1:n.624C>T

Select item 38683017511.

rs386830175 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: NT_167214.1:6257 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:6256:A:G
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NT_167214.1:g.6257A>G, XR_950600.3:n.3136T>C, XR_950600.2:n.2382T>C, XR_950600.1:n.1275T>C

Select item 38683017212.

rs386830172 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: NT_167214.1:6139 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:6138:G:A
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NT_167214.1:g.6139G>A, XR_950600.3:n.3254C>T, XR_950600.2:n.2500C>T, XR_950600.1:n.1393C>T

Select item 38683017013.

rs386830170 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: NT_167214.1:5950 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:5949:C:T
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NT_167214.1:g.5950C>T, XR_950600.3:n.3443G>A, XR_950600.2:n.2689G>A, XR_950600.1:n.1582G>A

Select item 38683016814.

rs386830168 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: NT_167214.1:5908 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:5907:T:C
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.5908T>C, XR_950600.3:n.3485A>G, XR_950600.2:n.2731A>G, XR_950600.1:n.1624A>G

Select item 38683016615.

rs386830166 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: NT_167214.1:5745 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:5744:A:G
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NT_167214.1:g.5745A>G, XR_950600.3:n.3648T>C, XR_950600.2:n.2894T>C, XR_950600.1:n.1787T>C

Select item 38683016416.

rs386830164 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: NT_167214.1:5726 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:5725:C:G
Gene:: LOC100507395 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NT_167214.1:g.5726C>G, XR_950600.3:n.3667G>C, XR_950600.2:n.2913G>C, XR_950600.1:n.1806G>C

Select item 38683015917.

rs386830159 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: NT_167214.1:5439 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:5438:A:G
Gene:: LOC100507395 (Varview)
Functional Consequence:: intron_variant
HGVS:: NT_167214.1:g.5439A>G

Select item 38683015718.

rs386830157 has merged into rs74199926 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: NT_167214.1:5348 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:5347:GGG:GG
Gene:: LOC100507395 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.5350del

Select item 38683015419.

rs386830154 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: NT_167214.1:4750 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:4749:G:A
Gene:: LOC100507395 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.4750G>A

Select item 38683015120.

rs386830151 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: NT_167214.1:4543 (GRCh38)
NT_167214.1:-1 (GRCh37)
Canonical SPDI:: NT_167214.1:4542:A:C
Gene:: LOC100507395 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by cluster
HGVS:: NT_167214.1:g.4543A>C