SNP Links for Gene (Select 474152) - SNP

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Links from Gene

Items: 19

Select item 14671571161.

rs1467157116 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:25184958 (GRCh38)
Y:27331105 (GRCh37)
Canonical SPDI:: NC_000024.10:25184957:G:C
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25184958G>C, NC_000024.9:g.27331105G>C, NG_004755.2:g.3374072G>C

Select item 14353596232.

rs1435359623 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:25185539 (GRCh38)
Y:27331686 (GRCh37)
Canonical SPDI:: NC_000024.10:25185538:T:C
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25185539T>C, NC_000024.9:g.27331686T>C, NG_004755.2:g.3374653T>C

Select item 13874592793.

rs1387459279 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:25185440 (GRCh38)
Y:27331587 (GRCh37)
Canonical SPDI:: NC_000024.10:25185439:A:G
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25185440A>G, NC_000024.9:g.27331587A>G, NG_004755.2:g.3374554A>G

Select item 13780980164.

rs1378098016 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:25184835 (GRCh38)
Y:27330982 (GRCh37)
Canonical SPDI:: NC_000024.10:25184834:G:A
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25184835G>A, NC_000024.9:g.27330982G>A, NG_004755.2:g.3373949G>A

Select item 12865518965.

rs1286551896 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:25185154 (GRCh38)
Y:27331301 (GRCh37)
Canonical SPDI:: NC_000024.10:25185153:C:T
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25185154C>T, NC_000024.9:g.27331301C>T, NG_004755.2:g.3374268C>T

Select item 5554630596.

rs555463059 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: Y:25186722 (GRCh38)
Y:27332869 (GRCh37)
Canonical SPDI:: NC_000024.10:25186721:T:A
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25186722T>A, NC_000024.9:g.27332869T>A, NG_004755.2:g.3375836T>A

Select item 3762384317.

rs376238431 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:25185139 (GRCh38)
Y:27331286 (GRCh37)
Canonical SPDI:: NC_000024.10:25185138:A:G
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.25185139A>G, NC_000024.9:g.27331286A>G, NG_004755.2:g.3374253A>G

Select item 1137496838.

rs113749683 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:25186622 (GRCh38)
Y:27332769 (GRCh37)
Canonical SPDI:: NC_000024.10:25186621:C:T
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25186622C>T, NC_000024.9:g.27332769C>T, NG_004755.2:g.3375736C>T

Select item 1131787869.

rs113178786 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: Y:25186303 (GRCh38)
Y:27332450 (GRCh37)
Canonical SPDI:: NC_000024.10:25186302:T:A
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25186303T>A, NC_000024.9:g.27332450T>A, NG_004755.2:g.3375417T>A

Select item 11301354710.

rs113013547 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: Y:25184272 (GRCh38)
Y:27330419 (GRCh37)
Canonical SPDI:: NC_000024.10:25184271:T:G
Gene:: TTTY17C (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.25184272T>G, NC_000024.9:g.27330419T>G, NG_004755.2:g.3373386T>G

Select item 11294401511.

rs112944015 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:25186331 (GRCh38)
Y:27332478 (GRCh37)
Canonical SPDI:: NC_000024.10:25186330:C:A
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25186331C>A, NC_000024.9:g.27332478C>A, NG_004755.2:g.3375445C>A

Select item 11271002012.

rs112710020 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:25185815 (GRCh38)
Y:27331962 (GRCh37)
Canonical SPDI:: NC_000024.10:25185814:T:C
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25185815T>C, NC_000024.9:g.27331962T>C, NG_004755.2:g.3374929T>C

Select item 11221843813.

rs112218438 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:25185060 (GRCh38)
Y:27331207 (GRCh37)
Canonical SPDI:: NC_000024.10:25185059:A:C
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25185060A>C, NC_000024.9:g.27331207A>C, NG_004755.2:g.3374174A>C

Select item 11182979514.

rs111829795 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:25186558 (GRCh38)
Y:27332705 (GRCh37)
Canonical SPDI:: NC_000024.10:25186557:G:T
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25186558G>T, NC_000024.9:g.27332705G>T, NG_004755.2:g.3375672G>T

Select item 11147491215.

rs111474912 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:25186530 (GRCh38)
Y:27332677 (GRCh37)
Canonical SPDI:: NC_000024.10:25186529:G:T
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25186530G>T, NC_000024.9:g.27332677G>T, NG_004755.2:g.3375644G>T

Select item 11136997216.

rs111369972 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:25186580 (GRCh38)
Y:27332727 (GRCh37)
Canonical SPDI:: NC_000024.10:25186579:A:G
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25186580A>G, NC_000024.9:g.27332727A>G, NG_004755.2:g.3375694A>G

Select item 15018617.

rs150186 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:25185497 (GRCh38)
Y:27331644 (GRCh37)
Canonical SPDI:: NC_000024.10:25185496:T:C
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.25185497T>C, NC_000024.9:g.27331644T>C, NG_004755.2:g.3374611T>C

Select item 15018518.

rs150185 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:25185904 (GRCh38)
Y:27332051 (GRCh37)
Canonical SPDI:: NC_000024.10:25185903:A:G
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.25185904A>G, NC_000024.9:g.27332051A>G, NG_004755.2:g.3375018A>G

Select item 15018419.

rs150184 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:25186072 (GRCh38)
Y:27332219 (GRCh37)
Canonical SPDI:: NC_000024.10:25186071:G:A
Gene:: TTTY17C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.25186072G>A, NC_000024.9:g.27332219G>A, NG_004755.2:g.3375186G>A