SNP Links for Gene (Select 5294) - SNP

Links from Gene

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Select item 14909395941.

rs1490939594 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:106887427 (GRCh38)
7:106527872 (GRCh37)
Canonical SPDI:: NC_000007.14:106887426:A:G
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.106887427A>G, NC_000007.13:g.106527872A>G, NG_050579.1:g.27150A>G

Select item 14909327942.

rs1490932794 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 7:106904833 (GRCh38)
7:106545278 (GRCh37)
Canonical SPDI:: NC_000007.14:106904832:A:T
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.106904833A>T, NC_000007.13:g.106545278A>T, NG_050579.1:g.44556A>T

Select item 14909110213.

rs1490911021 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 7:106869822 (GRCh38)
7:106510267 (GRCh37)
Canonical SPDI:: NC_000007.14:106869821:A:G,NC_000007.14:106869821:A:T
Gene:: PIK3CG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.106869822A>G, NC_000007.14:g.106869822A>T, NC_000007.13:g.106510267A>G, NC_000007.13:g.106510267A>T, NG_050579.1:g.9545A>G, NG_050579.1:g.9545A>T

Select item 14907927794.

rs1490792779 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:106882250 (GRCh38)
7:106522695 (GRCh37)
Canonical SPDI:: NC_000007.14:106882249:T:C
Gene:: PIK3CG (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.106882250T>C, NC_000007.13:g.106522695T>C, NG_050579.1:g.21973T>C

Select item 14906820055.

rs1490682005 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:106905395 (GRCh38)
7:106545840 (GRCh37)
Canonical SPDI:: NC_000007.14:106905394:G:A,NC_000007.14:106905394:G:C
Gene:: PIK3CG (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.106905395G>A, NC_000007.14:g.106905395G>C, NC_000007.13:g.106545840G>A, NC_000007.13:g.106545840G>C, NG_050579.1:g.45118G>A, NG_050579.1:g.45118G>C, NM_002649.3:c.*8G>A, NM_002649.3:c.*8G>C, NM_002649.2:c.*8G>A, NM_002649.2:c.*8G>C, NM_001282426.2:c.*8G>A, NM_001282426.2:c.*8G>C, NM_001282426.1:c.*8G>A, NM_001282426.1:c.*8G>C, NM_001282427.2:c.*8G>A, NM_001282427.2:c.*8G>C, NM_001282427.1:c.*8G>A, NM_001282427.1:c.*8G>C, XM_005250443.4:c.*8G>A, XM_005250443.4:c.*8G>C, XM_005250443.3:c.*8G>A, XM_005250443.3:c.*8G>C, XM_005250443.2:c.*8G>A, XM_005250443.2:c.*8G>C, XM_005250443.1:c.*8G>A, XM_005250443.1:c.*8G>C

Select item 14906762036.

rs1490676203 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 7:106876871 (GRCh38)
7:106517316 (GRCh37)
Canonical SPDI:: NC_000007.14:106876870:T:A,NC_000007.14:106876870:T:G
Gene:: PIK3CG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.106876871T>A, NC_000007.14:g.106876871T>G, NC_000007.13:g.106517316T>A, NC_000007.13:g.106517316T>G, NG_050579.1:g.16594T>A, NG_050579.1:g.16594T>G

Select item 14906508617.

rs1490650861 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:106877943 (GRCh38)
7:106518388 (GRCh37)
Canonical SPDI:: NC_000007.14:106877942:C:T
Gene:: PIK3CG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.106877943C>T, NC_000007.13:g.106518388C>T, NG_050579.1:g.17666C>T

Select item 14906220608.

rs1490622060 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:106893888 (GRCh38)
7:106534333 (GRCh37)
Canonical SPDI:: NC_000007.14:106893887:A:G
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.106893888A>G, NC_000007.13:g.106534333A>G, NG_050579.1:g.33611A>G

Select item 14904585469.

rs1490458546 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:106878734 (GRCh38)
7:106519179 (GRCh37)
Canonical SPDI:: NC_000007.14:106878733:C:A
Gene:: PIK3CG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.106878734C>A, NC_000007.13:g.106519179C>A, NG_050579.1:g.18457C>A

Select item 149042880010.

rs1490428800 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:106894885 (GRCh38)
7:106535330 (GRCh37)
Canonical SPDI:: NC_000007.14:106894884:C:A
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000007.14:g.106894885C>A, NC_000007.13:g.106535330C>A, NG_050579.1:g.34608C>A

Select item 149037197011.

rs1490371970 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:106896247 (GRCh38)
7:106536692 (GRCh37)
Canonical SPDI:: NC_000007.14:106896246:G:A
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.106896247G>A, NC_000007.13:g.106536692G>A, NG_050579.1:g.35970G>A

Select item 149023992312.

rs1490239923 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:106894437 (GRCh38)
7:106534882 (GRCh37)
Canonical SPDI:: NC_000007.14:106894436:T:G
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.106894437T>G, NC_000007.13:g.106534882T>G, NG_050579.1:g.34160T>G

Select item 149019094013.

rs1490190940 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 7:106886170 (GRCh38)
7:106526615 (GRCh37)
Canonical SPDI:: NC_000007.14:106886169:G:A,NC_000007.14:106886169:G:C,NC_000007.14:106886169:G:T
Gene:: PIK3CG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.106886170G>A, NC_000007.14:g.106886170G>C, NC_000007.14:g.106886170G>T, NC_000007.13:g.106526615G>A, NC_000007.13:g.106526615G>C, NC_000007.13:g.106526615G>T, NG_050579.1:g.25893G>A, NG_050579.1:g.25893G>C, NG_050579.1:g.25893G>T, NM_002649.3:c.2908G>A, NM_002649.3:c.2908G>C, NM_002649.3:c.2908G>T, NM_002649.2:c.2908G>A, NM_002649.2:c.2908G>C, NM_002649.2:c.2908G>T, NM_001282426.2:c.2908G>A, NM_001282426.2:c.2908G>C, NM_001282426.2:c.2908G>T, NM_001282426.1:c.2908G>A, NM_001282426.1:c.2908G>C, NM_001282426.1:c.2908G>T, NM_001282427.2:c.2908G>A, NM_001282427.2:c.2908G>C, NM_001282427.2:c.2908G>T, NM_001282427.1:c.2908G>A, NM_001282427.1:c.2908G>C, NM_001282427.1:c.2908G>T, XM_005250443.4:c.2908G>A, XM_005250443.4:c.2908G>C, XM_005250443.4:c.2908G>T, XM_005250443.3:c.2908G>A, XM_005250443.3:c.2908G>C, XM_005250443.3:c.2908G>T, XM_005250443.2:c.2908G>A, XM_005250443.2:c.2908G>C, XM_005250443.2:c.2908G>T, XM_005250443.1:c.2908G>A, XM_005250443.1:c.2908G>C, XM_005250443.1:c.2908G>T, XM_017012328.2:c.2908G>A, XM_017012328.2:c.2908G>C, XM_017012328.2:c.2908G>T, XM_017012328.1:c.2908G>A, XM_017012328.1:c.2908G>C, XM_017012328.1:c.2908G>T, XM_011516316.2:c.2908G>A, XM_011516316.2:c.2908G>C, XM_011516316.2:c.2908G>T, XM_011516316.1:c.2908G>A, XM_011516316.1:c.2908G>C, XM_011516316.1:c.2908G>T, XM_047420479.1:c.2908G>A, XM_047420479.1:c.2908G>C, XM_047420479.1:c.2908G>T, NP_002640.2:p.Gly970Arg, NP_002640.2:p.Gly970Arg, NP_002640.2:p.Gly970Trp, NP_001269355.1:p.Gly970Arg, NP_001269355.1:p.Gly970Arg, NP_001269355.1:p.Gly970Trp, NP_001269356.1:p.Gly970Arg, NP_001269356.1:p.Gly970Arg, NP_001269356.1:p.Gly970Trp, XP_005250500.1:p.Gly970Arg, XP_005250500.1:p.Gly970Arg, XP_005250500.1:p.Gly970Trp, XP_016867817.1:p.Gly970Arg, XP_016867817.1:p.Gly970Arg, XP_016867817.1:p.Gly970Trp, XP_011514618.1:p.Gly970Arg, XP_011514618.1:p.Gly970Arg, XP_011514618.1:p.Gly970Trp, XP_047276435.1:p.Gly970Arg, XP_047276435.1:p.Gly970Arg, XP_047276435.1:p.Gly970Trp

Select item 149009239814.

rs1490092398 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 7:106869255 (GRCh38)
7:106509700 (GRCh37)
Canonical SPDI:: NC_000007.14:106869254:A:C,NC_000007.14:106869254:A:G,NC_000007.14:106869254:A:T
Gene:: PIK3CG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.106869255A>C, NC_000007.14:g.106869255A>G, NC_000007.14:g.106869255A>T, NC_000007.13:g.106509700A>C, NC_000007.13:g.106509700A>G, NC_000007.13:g.106509700A>T, NG_050579.1:g.8978A>C, NG_050579.1:g.8978A>G, NG_050579.1:g.8978A>T, NM_002649.3:c.1694A>C, NM_002649.3:c.1694A>G, NM_002649.3:c.1694A>T, NM_002649.2:c.1694A>C, NM_002649.2:c.1694A>G, NM_002649.2:c.1694A>T, NM_001282426.2:c.1694A>C, NM_001282426.2:c.1694A>G, NM_001282426.2:c.1694A>T, NM_001282426.1:c.1694A>C, NM_001282426.1:c.1694A>G, NM_001282426.1:c.1694A>T, NM_001282427.2:c.1694A>C, NM_001282427.2:c.1694A>G, NM_001282427.2:c.1694A>T, NM_001282427.1:c.1694A>C, NM_001282427.1:c.1694A>G, NM_001282427.1:c.1694A>T, XM_005250443.4:c.1694A>C, XM_005250443.4:c.1694A>G, XM_005250443.4:c.1694A>T, XM_005250443.3:c.1694A>C, XM_005250443.3:c.1694A>G, XM_005250443.3:c.1694A>T, XM_005250443.2:c.1694A>C, XM_005250443.2:c.1694A>G, XM_005250443.2:c.1694A>T, XM_005250443.1:c.1694A>C, XM_005250443.1:c.1694A>G, XM_005250443.1:c.1694A>T, XM_017012328.2:c.1694A>C, XM_017012328.2:c.1694A>G, XM_017012328.2:c.1694A>T, XM_017012328.1:c.1694A>C, XM_017012328.1:c.1694A>G, XM_017012328.1:c.1694A>T, XM_011516316.2:c.1694A>C, XM_011516316.2:c.1694A>G, XM_011516316.2:c.1694A>T, XM_011516316.1:c.1694A>C, XM_011516316.1:c.1694A>G, XM_011516316.1:c.1694A>T, XM_011516317.2:c.1694A>C, XM_011516317.2:c.1694A>G, XM_011516317.2:c.1694A>T, XM_011516317.1:c.1694A>C, XM_011516317.1:c.1694A>G, XM_011516317.1:c.1694A>T, XM_047420479.1:c.1694A>C, XM_047420479.1:c.1694A>G, XM_047420479.1:c.1694A>T, XM_047420480.1:c.1694A>C, XM_047420480.1:c.1694A>G, XM_047420480.1:c.1694A>T, XM_047420481.1:c.1694A>C, XM_047420481.1:c.1694A>G, XM_047420481.1:c.1694A>T, NP_002640.2:p.Asn565Thr, NP_002640.2:p.Asn565Ser, NP_002640.2:p.Asn565Ile, NP_001269355.1:p.Asn565Thr, NP_001269355.1:p.Asn565Ser, NP_001269355.1:p.Asn565Ile, NP_001269356.1:p.Asn565Thr, NP_001269356.1:p.Asn565Ser, NP_001269356.1:p.Asn565Ile, XP_005250500.1:p.Asn565Thr, XP_005250500.1:p.Asn565Ser, XP_005250500.1:p.Asn565Ile, XP_016867817.1:p.Asn565Thr, XP_016867817.1:p.Asn565Ser, XP_016867817.1:p.Asn565Ile, XP_011514618.1:p.Asn565Thr, XP_011514618.1:p.Asn565Ser, XP_011514618.1:p.Asn565Ile, XP_011514619.1:p.Asn565Thr, XP_011514619.1:p.Asn565Ser, XP_011514619.1:p.Asn565Ile, XP_047276435.1:p.Asn565Thr, XP_047276435.1:p.Asn565Ser, XP_047276435.1:p.Asn565Ile, XP_047276436.1:p.Asn565Thr, XP_047276436.1:p.Asn565Ser, XP_047276436.1:p.Asn565Ile, XP_047276437.1:p.Asn565Thr, XP_047276437.1:p.Asn565Ser, XP_047276437.1:p.Asn565Ile

Select item 149006170215.

rs1490061702 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 7:106868238 (GRCh38)
7:106508683 (GRCh37)
Canonical SPDI:: NC_000007.14:106868237:G:A,NC_000007.14:106868237:G:C,NC_000007.14:106868237:G:T
Gene:: PIK3CG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.106868238G>A, NC_000007.14:g.106868238G>C, NC_000007.14:g.106868238G>T, NC_000007.13:g.106508683G>A, NC_000007.13:g.106508683G>C, NC_000007.13:g.106508683G>T, NG_050579.1:g.7961G>A, NG_050579.1:g.7961G>C, NG_050579.1:g.7961G>T, NM_002649.3:c.677G>A, NM_002649.3:c.677G>C, NM_002649.3:c.677G>T, NM_002649.2:c.677G>A, NM_002649.2:c.677G>C, NM_002649.2:c.677G>T, NM_001282426.2:c.677G>A, NM_001282426.2:c.677G>C, NM_001282426.2:c.677G>T, NM_001282426.1:c.677G>A, NM_001282426.1:c.677G>C, NM_001282426.1:c.677G>T, NM_001282427.2:c.677G>A, NM_001282427.2:c.677G>C, NM_001282427.2:c.677G>T, NM_001282427.1:c.677G>A, NM_001282427.1:c.677G>C, NM_001282427.1:c.677G>T, XM_005250443.4:c.677G>A, XM_005250443.4:c.677G>C, XM_005250443.4:c.677G>T, XM_005250443.3:c.677G>A, XM_005250443.3:c.677G>C, XM_005250443.3:c.677G>T, XM_005250443.2:c.677G>A, XM_005250443.2:c.677G>C, XM_005250443.2:c.677G>T, XM_005250443.1:c.677G>A, XM_005250443.1:c.677G>C, XM_005250443.1:c.677G>T, XM_017012328.2:c.677G>A, XM_017012328.2:c.677G>C, XM_017012328.2:c.677G>T, XM_017012328.1:c.677G>A, XM_017012328.1:c.677G>C, XM_017012328.1:c.677G>T, XM_011516316.2:c.677G>A, XM_011516316.2:c.677G>C, XM_011516316.2:c.677G>T, XM_011516316.1:c.677G>A, XM_011516316.1:c.677G>C, XM_011516316.1:c.677G>T, XM_011516317.2:c.677G>A, XM_011516317.2:c.677G>C, XM_011516317.2:c.677G>T, XM_011516317.1:c.677G>A, XM_011516317.1:c.677G>C, XM_011516317.1:c.677G>T, XM_047420479.1:c.677G>A, XM_047420479.1:c.677G>C, XM_047420479.1:c.677G>T, XM_047420480.1:c.677G>A, XM_047420480.1:c.677G>C, XM_047420480.1:c.677G>T, XM_047420481.1:c.677G>A, XM_047420481.1:c.677G>C, XM_047420481.1:c.677G>T, NP_002640.2:p.Arg226His, NP_002640.2:p.Arg226Pro, NP_002640.2:p.Arg226Leu, NP_001269355.1:p.Arg226His, NP_001269355.1:p.Arg226Pro, NP_001269355.1:p.Arg226Leu, NP_001269356.1:p.Arg226His, NP_001269356.1:p.Arg226Pro, NP_001269356.1:p.Arg226Leu, XP_005250500.1:p.Arg226His, XP_005250500.1:p.Arg226Pro, XP_005250500.1:p.Arg226Leu, XP_016867817.1:p.Arg226His, XP_016867817.1:p.Arg226Pro, XP_016867817.1:p.Arg226Leu, XP_011514618.1:p.Arg226His, XP_011514618.1:p.Arg226Pro, XP_011514618.1:p.Arg226Leu, XP_011514619.1:p.Arg226His, XP_011514619.1:p.Arg226Pro, XP_011514619.1:p.Arg226Leu, XP_047276435.1:p.Arg226His, XP_047276435.1:p.Arg226Pro, XP_047276435.1:p.Arg226Leu, XP_047276436.1:p.Arg226His, XP_047276436.1:p.Arg226Pro, XP_047276436.1:p.Arg226Leu, XP_047276437.1:p.Arg226His, XP_047276437.1:p.Arg226Pro, XP_047276437.1:p.Arg226Leu

Select item 149003387116.

rs1490033871 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 7:106884556 (GRCh38)
7:106525001 (GRCh37)
Canonical SPDI:: NC_000007.14:106884555:A:T
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.106884556A>T, NC_000007.13:g.106525001A>T, NG_050579.1:g.24279A>T

Select item 149000369717.

rs1490003697 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:106902514 (GRCh38)
7:106542959 (GRCh37)
Canonical SPDI:: NC_000007.14:106902513:A:G
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.106902514A>G, NC_000007.13:g.106542959A>G, NG_050579.1:g.42237A>G

Select item 148997145418.

rs1489971454 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:106880425 (GRCh38)
7:106520870 (GRCh37)
Canonical SPDI:: NC_000007.14:106880424:G:A
Gene:: PIK3CG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.106880425G>A, NC_000007.13:g.106520870G>A, NG_050579.1:g.20148G>A

Select item 148987136219.

rs1489871362 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:106883997 (GRCh38)
7:106524442 (GRCh37)
Canonical SPDI:: NC_000007.14:106883996:A:C
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.106883997A>C, NC_000007.13:g.106524442A>C, NG_050579.1:g.23720A>C

Select item 148980378820.

rs1489803788 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 7:106893326 (GRCh38)
7:106533771 (GRCh37)
Canonical SPDI:: NC_000007.14:106893325:A:
Gene:: PIK3CG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.106893326del, NC_000007.13:g.106533771del, NG_050579.1:g.33049del

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