SNP Links for Gene (Select 9721) - SNP

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:46555717 (GRCh38)
10:46993900 (GRCh37)
Canonical SPDI:: NC_000010.11:46555716:C:T
Gene:: GPRIN2 (Varview)
Functional Consequence:: upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.46555717C>T, NW_003871068.1:g.826832C>T, NC_000010.10:g.46993900G>A, NW_021160001.1:g.46898G>A, XM_047443204.1:c.-2652G>A

Select item 14899525838.

rs1489952583 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:46549192 (GRCh38)
10:47000425 (GRCh37)
Canonical SPDI:: NC_000010.11:46549191:G:A,NC_000010.11:46549191:G:T
Gene:: GPRIN2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.46549192G>A, NC_000010.11:g.46549192G>T, NW_003871068.1:g.820307G>A, NW_003871068.1:g.820307G>T, NC_000010.10:g.47000425C>T, NC_000010.10:g.47000425C>A, NW_021160001.1:g.53416C>T, NW_021160001.1:g.53416C>A, NM_014696.5:c.*168C>T, NM_014696.5:c.*168C>A, NM_014696.4:c.*168C>T, NM_014696.4:c.*168C>A, NM_014696.3:c.*168C>T, NM_014696.3:c.*168C>A, XM_017016976.3:c.*168C>T, XM_017016976.3:c.*168C>A, XM_017016976.2:c.*168C>T, XM_017016976.2:c.*168C>A, XM_017016976.1:c.*168C>T, XM_017016976.1:c.*168C>A, XM_017016983.3:c.*168C>T, XM_017016983.3:c.*168C>A, XM_017016983.2:c.*168C>T, XM_017016983.2:c.*168C>A, XM_017016983.1:c.*168C>T, XM_017016983.1:c.*168C>A, XM_017016984.3:c.*168C>T, XM_017016984.3:c.*168C>A, XM_017016984.2:c.*168C>T, XM_017016984.2:c.*168C>A, XM_017016984.1:c.*168C>T, XM_017016984.1:c.*168C>A, XM_017016974.3:c.*168C>T, XM_017016974.3:c.*168C>A, XM_017016974.2:c.*168C>T, XM_017016974.2:c.*168C>A, XM_017016974.1:c.*168C>T, XM_017016974.1:c.*168C>A, XM_017016982.3:c.*168C>T, XM_017016982.3:c.*168C>A, XM_017016982.2:c.*168C>T, XM_017016982.2:c.*168C>A, XM_017016982.1:c.*168C>T, XM_017016982.1:c.*168C>A, XM_017016978.3:c.*168C>T, XM_017016978.3:c.*168C>A, XM_017016978.2:c.*168C>T, XM_017016978.2:c.*168C>A, XM_017016978.1:c.*168C>T, XM_017016978.1:c.*168C>A, XM_017016981.3:c.*168C>T, XM_017016981.3:c.*168C>A, XM_017016981.2:c.*168C>T, XM_017016981.2:c.*168C>A, XM_017016981.1:c.*168C>T, XM_017016981.1:c.*168C>A, XM_017016975.3:c.*168C>T, XM_017016975.3:c.*168C>A, XM_017016975.2:c.*168C>T, XM_017016975.2:c.*168C>A, XM_017016975.1:c.*168C>T, XM_017016975.1:c.*168C>A, XM_017016977.3:c.*168C>T, XM_017016977.3:c.*168C>A, XM_017016977.2:c.*168C>T, XM_017016977.2:c.*168C>A, XM_017016977.1:c.*168C>T, XM_017016977.1:c.*168C>A, NM_001394744.1:c.*168C>T, NM_001394744.1:c.*168C>A, NM_001385299.1:c.*168C>T, NM_001385299.1:c.*168C>A, NM_001385298.1:c.*168C>T, NM_001385298.1:c.*168C>A, NM_001394741.1:c.*168C>T, NM_001394741.1:c.*168C>A, NM_001394740.1:c.*168C>T, NM_001394740.1:c.*168C>A, NM_001394743.1:c.*168C>T, NM_001394743.1:c.*168C>A, NM_001394742.1:c.*168C>T, NM_001394742.1:c.*168C>A, NM_001385297.1:c.*168C>T, NM_001385297.1:c.*168C>A, NM_001385301.1:c.*168C>T, NM_001385301.1:c.*168C>A, NM_001385296.1:c.*168C>T, NM_001385296.1:c.*168C>A, NM_001394739.1:c.*168C>T, NM_001394739.1:c.*168C>A, NM_001385295.1:c.*168C>T, NM_001385295.1:c.*168C>A, NM_001385294.1:c.*168C>T, NM_001385294.1:c.*168C>A, NM_001385293.1:c.*168C>T, NM_001385293.1:c.*168C>A, NM_001385291.1:c.*168C>T, NM_001385291.1:c.*168C>A, NM_001385283.1:c.*168C>T, NM_001385283.1:c.*168C>A, NM_001385281.1:c.*168C>T, NM_001385281.1:c.*168C>A, NM_001385287.1:c.*168C>T, NM_001385287.1:c.*168C>A, NM_001385300.1:c.*168C>T, NM_001385300.1:c.*168C>A, NM_001385280.1:c.*168C>T, NM_001385280.1:c.*168C>A, NM_001385289.1:c.*168C>T, NM_001385289.1:c.*168C>A, NM_001385279.1:c.*168C>T, NM_001385279.1:c.*168C>A, NM_001385278.1:c.*168C>T, NM_001385278.1:c.*168C>A, NM_001385277.1:c.*168C>T, NM_001385277.1:c.*168C>A, NM_001385282.1:c.*168C>T, NM_001385282.1:c.*168C>A, NM_001385276.1:c.*168C>T, NM_001385276.1:c.*168C>A, NM_001385275.1:c.*168C>T, NM_001385275.1:c.*168C>A, XM_047443204.1:c.*168C>T, XM_047443204.1:c.*168C>A

Select item 14899306559.

rs1489930655 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:46558556 (GRCh38)
10:46991061 (GRCh37)
Canonical SPDI:: NC_000010.11:46558555:A:G
Gene:: GPRIN2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.46558556A>G, NW_003871068.1:g.829671A>G, NC_000010.10:g.46991061T>C, NW_021160001.1:g.44061T>C

Select item 148989876910.

rs1489898769 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:46558012 (GRCh38)
10:46991605 (GRCh37)
Canonical SPDI:: NC_000010.11:46558011:G:A,NC_000010.11:46558011:G:C
Gene:: GPRIN2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00039/11 (TOMMO)
C=0.00055/1 (Korea1K)
HGVS:: NC_000010.11:g.46558012G>A, NC_000010.11:g.46558012G>C, NW_003871068.1:g.829127G>A, NW_003871068.1:g.829127G>C, NC_000010.10:g.46991605C>T, NC_000010.10:g.46991605C>G, NW_021160001.1:g.44605C>T, NW_021160001.1:g.44605C>G

Select item 148976778211.

rs1489767782 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:46557960 (GRCh38)
10:46991657 (GRCh37)
Canonical SPDI:: NC_000010.11:46557959:A:G
Gene:: GPRIN2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.00008/1 (ALFA)
HGVS:: NC_000010.11:g.46557960A>G, NW_003871068.1:g.829075A>G, NC_000010.10:g.46991657T>C, NW_021160001.1:g.44657T>C

Select item 148975434812.

rs1489754348 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:46545166 (GRCh38)
10:47004451 (GRCh37)
Canonical SPDI:: NC_000010.11:46545165:T:C
Gene:: GPRIN2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.46545166T>C, NW_003871068.1:g.816281T>C, NC_000010.10:g.47004451A>G, NW_021160001.1:g.57436A>G, NM_014696.5:c.*4194A>G, NM_014696.4:c.*4194A>G, XM_017016976.3:c.*4194A>G, XM_017016976.2:c.*4194A>G, XM_017016976.1:c.*4194A>G, XM_017016983.3:c.*4194A>G, XM_017016983.2:c.*4194A>G, XM_017016983.1:c.*4194A>G, XM_017016984.3:c.*4194A>G, XM_017016984.2:c.*4194A>G, XM_017016984.1:c.*4194A>G, XM_017016974.3:c.*4194A>G, XM_017016974.2:c.*4194A>G, XM_017016974.1:c.*4194A>G, XM_017016982.3:c.*4194A>G, XM_017016982.2:c.*4194A>G, XM_017016982.1:c.*4194A>G, XM_017016978.3:c.*4194A>G, XM_017016978.2:c.*4194A>G, XM_017016978.1:c.*4194A>G, XM_017016981.3:c.*4194A>G, XM_017016981.2:c.*4194A>G, XM_017016981.1:c.*4194A>G, XM_017016975.3:c.*4194A>G, XM_017016975.2:c.*4194A>G, XM_017016975.1:c.*4194A>G, XM_017016977.3:c.*4194A>G, XM_017016977.2:c.*4194A>G, XM_017016977.1:c.*4194A>G, NM_001394744.1:c.*4194A>G, NM_001385299.1:c.*4194A>G, NM_001385298.1:c.*4194A>G, NM_001394741.1:c.*4194A>G, NM_001394740.1:c.*4194A>G, NM_001394743.1:c.*4194A>G, NM_001394742.1:c.*4194A>G, NM_001385297.1:c.*4194A>G, NM_001385301.1:c.*4194A>G, NM_001385296.1:c.*4194A>G, NM_001394739.1:c.*4194A>G, NM_001385295.1:c.*4194A>G, NM_001385294.1:c.*4194A>G, NM_001385293.1:c.*4194A>G, NM_001385291.1:c.*4194A>G, NM_001385283.1:c.*4194A>G, NM_001385281.1:c.*4194A>G, NM_001385287.1:c.*4194A>G, NM_001385300.1:c.*4194A>G, NM_001385280.1:c.*4194A>G, NM_001385289.1:c.*4194A>G, NM_001385279.1:c.*4194A>G, NM_001385278.1:c.*4194A>G, NM_001385277.1:c.*4194A>G, NM_001385282.1:c.*4194A>G, NM_001385276.1:c.*4194A>G, NM_001385275.1:c.*4194A>G, XM_047443204.1:c.*4188A>G

Select item 148966069913.

rs1489660699 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:46549649 (GRCh38)
10:46999968 (GRCh37)
Canonical SPDI:: NC_000010.11:46549648:A:G
Gene:: GPRIN2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.46549649A>G, NW_003871068.1:g.820764A>G, NC_000010.10:g.46999968T>C, NW_021160001.1:g.52959T>C, NM_014696.5:c.1088T>C, NM_014696.4:c.1088T>C, NM_014696.3:c.1088T>C, XM_017016976.3:c.1160T>C, XM_017016976.2:c.1160T>C, XM_017016976.1:c.1160T>C, XM_017016983.3:c.1160T>C, XM_017016983.2:c.1160T>C, XM_017016983.1:c.1160T>C, XM_017016984.3:c.1160T>C, XM_017016984.2:c.1160T>C, XM_017016984.1:c.1160T>C, XM_017016974.3:c.1160T>C, XM_017016974.2:c.1160T>C, XM_017016974.1:c.1160T>C, XM_017016982.3:c.1160T>C, XM_017016982.2:c.1160T>C, XM_017016982.1:c.1160T>C, XM_017016978.3:c.1160T>C, XM_017016978.2:c.1160T>C, XM_017016978.1:c.1160T>C, XM_017016981.3:c.1160T>C, XM_017016981.2:c.1160T>C, XM_017016981.1:c.1160T>C, XM_017016975.3:c.1160T>C, XM_017016975.2:c.1160T>C, XM_017016975.1:c.1160T>C, XM_017016977.3:c.1160T>C, XM_017016977.2:c.1160T>C, XM_017016977.1:c.1160T>C, NM_001394744.1:c.1160T>C, NM_001385299.1:c.1160T>C, NM_001385298.1:c.1160T>C, NM_001394741.1:c.1088T>C, NM_001394740.1:c.1088T>C, NM_001394743.1:c.1160T>C, NM_001394742.1:c.1160T>C, NM_001385297.1:c.1160T>C, NM_001385301.1:c.1160T>C, NM_001385296.1:c.1160T>C, NM_001394739.1:c.1088T>C, NM_001385295.1:c.1160T>C, NM_001385294.1:c.1160T>C, NM_001385293.1:c.1160T>C, NM_001385291.1:c.1160T>C, NM_001385283.1:c.1088T>C, NM_001385281.1:c.1088T>C, NM_001385287.1:c.1160T>C, NM_001385300.1:c.1160T>C, NM_001385280.1:c.1088T>C, NM_001385289.1:c.1160T>C, NM_001385279.1:c.1088T>C, NM_001385278.1:c.1088T>C, NM_001385277.1:c.1088T>C, NM_001385282.1:c.1088T>C, NM_001385276.1:c.1088T>C, NM_001385275.1:c.1088T>C, XM_047443204.1:c.1160T>C, NP_055511.2:p.Phe363Ser, XP_016872465.1:p.Phe387Ser, XP_016872472.1:p.Phe387Ser, XP_016872473.1:p.Phe387Ser, XP_016872463.1:p.Phe387Ser, XP_016872471.1:p.Phe387Ser, XP_016872467.1:p.Phe387Ser, XP_016872470.1:p.Phe387Ser, XP_016872464.1:p.Phe387Ser, XP_016872466.1:p.Phe387Ser, NP_001381673.1:p.Phe387Ser, NP_001372228.1:p.Phe387Ser, NP_001372227.1:p.Phe387Ser, NP_001381670.1:p.Phe363Ser, NP_001381669.1:p.Phe363Ser, NP_001381672.1:p.Phe387Ser, NP_001381671.1:p.Phe387Ser, NP_001372226.1:p.Phe387Ser, NP_001372230.1:p.Phe387Ser, NP_001372225.1:p.Phe387Ser, NP_001381668.1:p.Phe363Ser, NP_001372224.1:p.Phe387Ser, NP_001372223.1:p.Phe387Ser, NP_001372222.1:p.Phe387Ser, NP_001372220.1:p.Phe387Ser, NP_001372212.1:p.Phe363Ser, NP_001372210.1:p.Phe363Ser, NP_001372216.1:p.Phe387Ser, NP_001372229.1:p.Phe387Ser, NP_001372209.1:p.Phe363Ser, NP_001372218.1:p.Phe387Ser, NP_001372208.1:p.Phe363Ser, NP_001372207.1:p.Phe363Ser, NP_001372206.1:p.Phe363Ser, NP_001372211.1:p.Phe363Ser, NP_001372205.1:p.Phe363Ser, NP_001372204.1:p.Phe363Ser

Select item 148961656914.

rs1489616569 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:46551463 (GRCh38)
10:46998154 (GRCh37)
Canonical SPDI:: NC_000010.11:46551462:T:A
Gene:: GPRIN2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000084/1 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.46551463T>A, NW_003871068.1:g.822578T>A, NC_000010.10:g.46998154A>T, NW_021160001.1:g.51149A>T, XM_017016976.3:c.19A>T, XM_017016976.2:c.19A>T, XM_017016976.1:c.19A>T, XM_017016983.3:c.19A>T, XM_017016983.2:c.19A>T, XM_017016983.1:c.19A>T, XM_017016984.3:c.19A>T, XM_017016984.2:c.19A>T, XM_017016984.1:c.19A>T, XM_017016974.3:c.19A>T, XM_017016974.2:c.19A>T, XM_017016974.1:c.19A>T, XM_017016982.3:c.19A>T, XM_017016982.2:c.19A>T, XM_017016982.1:c.19A>T, XM_017016978.3:c.19A>T, XM_017016978.2:c.19A>T, XM_017016978.1:c.19A>T, XM_017016981.3:c.19A>T, XM_017016981.2:c.19A>T, XM_017016981.1:c.19A>T, XM_017016975.3:c.19A>T, XM_017016975.2:c.19A>T, XM_017016975.1:c.19A>T, XM_017016977.3:c.19A>T, XM_017016977.2:c.19A>T, XM_017016977.1:c.19A>T, NM_001394744.1:c.19A>T, NM_001385299.1:c.19A>T, NM_001385298.1:c.19A>T, NM_001394743.1:c.19A>T, NM_001394742.1:c.19A>T, NM_001385297.1:c.19A>T, NM_001385301.1:c.19A>T, NM_001385296.1:c.19A>T, NM_001385295.1:c.19A>T, NM_001385294.1:c.19A>T, NM_001385293.1:c.19A>T, NM_001385291.1:c.19A>T, NM_001385287.1:c.19A>T, NM_001385300.1:c.19A>T, NM_001385289.1:c.19A>T, XM_047443204.1:c.19A>T, XP_016872465.1:p.Met7Leu, XP_016872472.1:p.Met7Leu, XP_016872473.1:p.Met7Leu, XP_016872463.1:p.Met7Leu, XP_016872471.1:p.Met7Leu, XP_016872467.1:p.Met7Leu, XP_016872470.1:p.Met7Leu, XP_016872464.1:p.Met7Leu, XP_016872466.1:p.Met7Leu, NP_001381673.1:p.Met7Leu, NP_001372228.1:p.Met7Leu, NP_001372227.1:p.Met7Leu, NP_001381672.1:p.Met7Leu, NP_001381671.1:p.Met7Leu, NP_001372226.1:p.Met7Leu, NP_001372230.1:p.Met7Leu, NP_001372225.1:p.Met7Leu, NP_001372224.1:p.Met7Leu, NP_001372223.1:p.Met7Leu, NP_001372222.1:p.Met7Leu, NP_001372220.1:p.Met7Leu, NP_001372216.1:p.Met7Leu, NP_001372229.1:p.Met7Leu, NP_001372218.1:p.Met7Leu

Select item 148943109815.

rs1489431098 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:46544894 (GRCh38)
10:47004723 (GRCh37)
Canonical SPDI:: NC_000010.11:46544893:C:T
Gene:: GPRIN2 (Varview)
Functional Consequence:: 3_prime_UTR_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_000010.11:g.46544894C>T, NW_003871068.1:g.816009C>T, NC_000010.10:g.47004723G>A, NW_021160001.1:g.57708G>A, NM_014696.5:c.*4466G>A, NM_014696.4:c.*4466G>A, XM_017016976.3:c.*4466G>A, XM_017016976.2:c.*4466G>A, XM_017016976.1:c.*4466G>A, XM_017016983.3:c.*4466G>A, XM_017016983.2:c.*4466G>A, XM_017016983.1:c.*4466G>A, XM_017016984.3:c.*4466G>A, XM_017016984.2:c.*4466G>A, XM_017016984.1:c.*4466G>A, XM_017016974.3:c.*4466G>A, XM_017016974.2:c.*4466G>A, XM_017016974.1:c.*4466G>A, XM_017016982.3:c.*4466G>A, XM_017016982.2:c.*4466G>A, XM_017016982.1:c.*4466G>A, XM_017016978.3:c.*4466G>A, XM_017016978.2:c.*4466G>A, XM_017016978.1:c.*4466G>A, XM_017016981.3:c.*4466G>A, XM_017016981.2:c.*4466G>A, XM_017016981.1:c.*4466G>A, XM_017016975.3:c.*4466G>A, XM_017016975.2:c.*4466G>A, XM_017016975.1:c.*4466G>A, XM_017016977.3:c.*4466G>A, XM_017016977.2:c.*4466G>A, XM_017016977.1:c.*4466G>A, NM_001394744.1:c.*4466G>A, NM_001385299.1:c.*4466G>A, NM_001385298.1:c.*4466G>A, NM_001394741.1:c.*4466G>A, NM_001394740.1:c.*4466G>A, NM_001394743.1:c.*4466G>A, NM_001394742.1:c.*4466G>A, NM_001385297.1:c.*4466G>A, NM_001385301.1:c.*4466G>A, NM_001385296.1:c.*4466G>A, NM_001394739.1:c.*4466G>A, NM_001385295.1:c.*4466G>A, NM_001385294.1:c.*4466G>A, NM_001385293.1:c.*4466G>A, NM_001385291.1:c.*4466G>A, NM_001385283.1:c.*4466G>A, NM_001385281.1:c.*4466G>A, NM_001385287.1:c.*4466G>A, NM_001385300.1:c.*4466G>A, NM_001385280.1:c.*4466G>A, NM_001385289.1:c.*4466G>A, NM_001385279.1:c.*4466G>A, NM_001385278.1:c.*4466G>A, NM_001385277.1:c.*4466G>A, NM_001385282.1:c.*4466G>A, NM_001385276.1:c.*4466G>A, NM_001385275.1:c.*4466G>A, XM_047443204.1:c.*4460G>A

Select item 148941109316.

rs1489411093 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:46545156 (GRCh38)
10:47004461 (GRCh37)
Canonical SPDI:: NC_000010.11:46545155:T:C
Gene:: GPRIN2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
C=0.000312/2 (1000Genomes)
HGVS:: NC_000010.11:g.46545156T>C, NW_003871068.1:g.816271T>C, NC_000010.10:g.47004461A>G, NW_021160001.1:g.57446A>G, NM_014696.5:c.*4204A>G, NM_014696.4:c.*4204A>G, XM_017016976.3:c.*4204A>G, XM_017016976.2:c.*4204A>G, XM_017016976.1:c.*4204A>G, XM_017016983.3:c.*4204A>G, XM_017016983.2:c.*4204A>G, XM_017016983.1:c.*4204A>G, XM_017016984.3:c.*4204A>G, XM_017016984.2:c.*4204A>G, XM_017016984.1:c.*4204A>G, XM_017016974.3:c.*4204A>G, XM_017016974.2:c.*4204A>G, XM_017016974.1:c.*4204A>G, XM_017016982.3:c.*4204A>G, XM_017016982.2:c.*4204A>G, XM_017016982.1:c.*4204A>G, XM_017016978.3:c.*4204A>G, XM_017016978.2:c.*4204A>G, XM_017016978.1:c.*4204A>G, XM_017016981.3:c.*4204A>G, XM_017016981.2:c.*4204A>G, XM_017016981.1:c.*4204A>G, XM_017016975.3:c.*4204A>G, XM_017016975.2:c.*4204A>G, XM_017016975.1:c.*4204A>G, XM_017016977.3:c.*4204A>G, XM_017016977.2:c.*4204A>G, XM_017016977.1:c.*4204A>G, NM_001394744.1:c.*4204A>G, NM_001385299.1:c.*4204A>G, NM_001385298.1:c.*4204A>G, NM_001394741.1:c.*4204A>G, NM_001394740.1:c.*4204A>G, NM_001394743.1:c.*4204A>G, NM_001394742.1:c.*4204A>G, NM_001385297.1:c.*4204A>G, NM_001385301.1:c.*4204A>G, NM_001385296.1:c.*4204A>G, NM_001394739.1:c.*4204A>G, NM_001385295.1:c.*4204A>G, NM_001385294.1:c.*4204A>G, NM_001385293.1:c.*4204A>G, NM_001385291.1:c.*4204A>G, NM_001385283.1:c.*4204A>G, NM_001385281.1:c.*4204A>G, NM_001385287.1:c.*4204A>G, NM_001385300.1:c.*4204A>G, NM_001385280.1:c.*4204A>G, NM_001385289.1:c.*4204A>G, NM_001385279.1:c.*4204A>G, NM_001385278.1:c.*4204A>G, NM_001385277.1:c.*4204A>G, NM_001385282.1:c.*4204A>G, NM_001385276.1:c.*4204A>G, NM_001385275.1:c.*4204A>G, XM_047443204.1:c.*4198A>G

Select item 148936420017.

rs1489364200 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:46553831 (GRCh38)
10:46995786 (GRCh37)
Canonical SPDI:: NC_000010.11:46553830:A:G
Gene:: GPRIN2 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000036/5 (GnomAD)
HGVS:: NC_000010.11:g.46553831A>G, NW_003871068.1:g.824946A>G, NC_000010.10:g.46995786T>C, NW_021160001.1:g.48781T>C, XM_017016976.3:c.-1964T>C, XM_017016976.2:c.-1964T>C, XM_017016976.1:c.-1964T>C, XM_017016983.3:c.-1964T>C, XM_017016983.2:c.-1964T>C, XM_017016983.1:c.-1964T>C, XM_017016984.3:c.-1964T>C, XM_017016984.2:c.-1964T>C, XM_017016984.1:c.-1964T>C, XM_017016974.3:c.-1964T>C, XM_017016974.2:c.-1964T>C, XM_017016974.1:c.-1964T>C, XM_017016982.3:c.-1964T>C, XM_017016982.2:c.-1964T>C, XM_017016982.1:c.-1964T>C, XM_017016978.3:c.-1964T>C, XM_017016978.2:c.-1964T>C, XM_017016978.1:c.-1964T>C, XM_017016981.3:c.-1964T>C, XM_017016981.2:c.-1964T>C, XM_017016981.1:c.-1964T>C, XM_017016975.3:c.-1926T>C, XM_017016975.2:c.-1926T>C, XM_017016975.1:c.-1926T>C, XM_047443204.1:c.-1964T>C

Select item 148932897118.

rs1489328971 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:46544324 (GRCh38)
10:47005293 (GRCh37)
Canonical SPDI:: NC_000010.11:46544323:T:G
Gene:: GPRIN2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.46544324T>G, NW_003871068.1:g.815439T>G, NC_000010.10:g.47005293A>C, NW_021160001.1:g.58278A>C, NM_014696.5:c.*5036A>C, NM_014696.4:c.*5036A>C, XM_017016976.3:c.*5036A>C, XM_017016976.2:c.*5036A>C, XM_017016976.1:c.*5036A>C, XM_017016983.3:c.*5036A>C, XM_017016983.2:c.*5036A>C, XM_017016983.1:c.*5036A>C, XM_017016984.3:c.*5036A>C, XM_017016984.2:c.*5036A>C, XM_017016984.1:c.*5036A>C, XM_017016974.3:c.*5036A>C, XM_017016974.2:c.*5036A>C, XM_017016974.1:c.*5036A>C, XM_017016982.3:c.*5036A>C, XM_017016982.2:c.*5036A>C, XM_017016982.1:c.*5036A>C, XM_017016978.3:c.*5036A>C, XM_017016978.2:c.*5036A>C, XM_017016978.1:c.*5036A>C, XM_017016981.3:c.*5036A>C, XM_017016981.2:c.*5036A>C, XM_017016981.1:c.*5036A>C, XM_017016975.3:c.*5036A>C, XM_017016975.2:c.*5036A>C, XM_017016975.1:c.*5036A>C, XM_017016977.3:c.*5036A>C, XM_017016977.2:c.*5036A>C, XM_017016977.1:c.*5036A>C, NM_001394744.1:c.*5036A>C, NM_001385299.1:c.*5036A>C, NM_001385298.1:c.*5036A>C, NM_001394741.1:c.*5036A>C, NM_001394740.1:c.*5036A>C, NM_001394743.1:c.*5036A>C, NM_001394742.1:c.*5036A>C, NM_001385297.1:c.*5036A>C, NM_001385301.1:c.*5036A>C, NM_001385296.1:c.*5036A>C, NM_001394739.1:c.*5036A>C, NM_001385295.1:c.*5036A>C, NM_001385294.1:c.*5036A>C, NM_001385293.1:c.*5036A>C, NM_001385291.1:c.*5036A>C, NM_001385283.1:c.*5036A>C, NM_001385281.1:c.*5036A>C, NM_001385287.1:c.*5036A>C, NM_001385300.1:c.*5036A>C, NM_001385280.1:c.*5036A>C, NM_001385289.1:c.*5036A>C, NM_001385279.1:c.*5036A>C, NM_001385278.1:c.*5036A>C, NM_001385277.1:c.*5036A>C, NM_001385282.1:c.*5036A>C, NM_001385276.1:c.*5036A>C, NM_001385275.1:c.*5036A>C, XM_047443204.1:c.*5030A>C

Select item 148889499219.

rs1488894992 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:46554543 (GRCh38)
10:46995074 (GRCh37)
Canonical SPDI:: NC_000010.11:46554542:A:T
Gene:: GPRIN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000084/1 (ALFA)
T=0.000071/10 (GnomAD)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000010.11:g.46554543A>T, NW_003871068.1:g.825658A>T, NC_000010.10:g.46995074T>A, NW_021160001.1:g.48071T>A

Select item 148852780320.

rs1488527803 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAG>- [Show Flanks]
Chromosome:: 10:46556234 (GRCh38)
10:46993382 (GRCh37)
Canonical SPDI:: NC_000010.11:46556232:GAAG:G
Gene:: GPRIN2 (Varview)
Functional Consequence:: upstream_transcript_variant,genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
-=0.000057/8 (GnomAD)
HGVS:: NC_000010.11:g.46556234_46556236del, NW_003871068.1:g.827349_827351del, NC_000010.10:g.46993382_46993384del, NW_021160001.1:g.46380_46382del, NM_014696.5:c.-299_-297del, XM_017016976.3:c.-2646_-2644del, XM_017016976.2:c.-2646_-2644del, XM_017016976.1:c.-2646_-2644del, XM_017016983.3:c.-2507_-2505del, XM_017016983.2:c.-2507_-2505del, XM_017016983.1:c.-2507_-2505del, XM_017016984.3:c.-2491_-2489del, XM_017016984.2:c.-2491_-2489del, XM_017016984.1:c.-2491_-2489del, NM_001394744.1:c.-542_-540del, NM_001394741.1:c.-470_-468del, NM_001394740.1:c.-454_-452del, NM_001394743.1:c.-365_-363del, NM_001394742.1:c.-349_-347del, NM_001394739.1:c.-315_-313del

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