SNP Links for Gene (Select 389090) - SNP

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Select item 14912586391.

rs1491258639 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTTTTTTTTT [Show Flanks]
Chromosome:: 2:240029536 (GRCh38)
2:240968954 (GRCh37)
Canonical SPDI:: NC_000002.12:240029536:TT:TTTTTTTTTTTT
Gene:: OR6B2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
HGVS:: NC_000002.12:g.240029538_240029539insTTTTTTTTTT, NC_000002.11:g.240968955_240968956insTTTTTTTTTT, NG_031855.2:g.866_867insAAAAAAAAAA, NM_001005853.1:c.893_894insAAAAAAAAAA, NM_001001962.1:c.893_894insAAAAAAAAAA, NP_001005853.1:p.Asp299fs

Select item 14911038102.

rs1491103810 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 2:240029536 (GRCh38)
2:240968953 (GRCh37)
Canonical SPDI:: NC_000002.12:240029535:CT:
Gene:: OR6B2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.240029536_240029537del, NC_000002.11:g.240968953_240968954del, NG_031855.2:g.866_867del, NM_001005853.1:c.893_894del, NM_001001962.1:c.893_894del, NP_001005853.1:p.Lys298fs

Select item 14898163063.

rs1489816306 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:240030573 (GRCh38)
2:240969990 (GRCh37)
Canonical SPDI:: NC_000002.12:240030572:C:A
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.240030573C>A, NC_000002.11:g.240969990C>A

Select item 14878998324.

rs1487899832 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:240029473 (GRCh38)
2:240968890 (GRCh37)
Canonical SPDI:: NC_000002.12:240029472:C:G
Gene:: OR6B2 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
HGVS:: NC_000002.12:g.240029473C>G, NC_000002.11:g.240968890C>G, NG_031855.2:g.930G>C, NM_001001962.1:c.*18G>C

Select item 14872411665.

rs1487241166 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:240032193 (GRCh38)
2:240971610 (GRCh37)
Canonical SPDI:: NC_000002.12:240032192:G:A
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.240032193G>A, NC_000002.11:g.240971610G>A

Select item 14868199656.

rs1486819965 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:240031924 (GRCh38)
2:240971341 (GRCh37)
Canonical SPDI:: NC_000002.12:240031923:G:A
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000002.12:g.240031924G>A, NC_000002.11:g.240971341G>A

Select item 14858982217.

rs1485898221 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 2:240032077 (GRCh38)
2:240971494 (GRCh37)
Canonical SPDI:: NC_000002.12:240032076:T:A,NC_000002.12:240032076:T:C
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00032/5 (TOMMO)
C=0.00068/2 (KOREAN)
C=0.00109/2 (Korea1K)
HGVS:: NC_000002.12:g.240032077T>A, NC_000002.12:g.240032077T>C, NC_000002.11:g.240971494T>A, NC_000002.11:g.240971494T>C

Select item 14857824088.

rs1485782408 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 2:240029553 (GRCh38)
2:240968970 (GRCh37)
Canonical SPDI:: NC_000002.12:240029552:T:
Gene:: OR6B2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000002.12:g.240029553del, NC_000002.11:g.240968970del, NG_031855.2:g.850del, NM_001005853.1:c.877del, NM_001001962.1:c.877del, NP_001005853.1:p.Arg293fs

Select item 14855416109.

rs1485541610 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:240032409 (GRCh38)
2:240971826 (GRCh37)
Canonical SPDI:: NC_000002.12:240032408:G:A
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.240032409G>A, NC_000002.11:g.240971826G>A

Select item 148427475210.

rs1484274752 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:240030972 (GRCh38)
2:240970389 (GRCh37)
Canonical SPDI:: NC_000002.12:240030971:C:T
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.240030972C>T, NC_000002.11:g.240970389C>T

Select item 148393560111.

rs1483935601 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:240030620 (GRCh38)
2:240970037 (GRCh37)
Canonical SPDI:: NC_000002.12:240030619:A:G
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.240030620A>G, NC_000002.11:g.240970037A>G

Select item 148354879012.

rs1483548790 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:240031216 (GRCh38)
2:240970633 (GRCh37)
Canonical SPDI:: NC_000002.12:240031215:C:T
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000002.12:g.240031216C>T, NC_000002.11:g.240970633C>T

Select item 148270430013.

rs1482704300 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 2:240030495 (GRCh38)
2:240969912 (GRCh37)
Canonical SPDI:: NC_000002.12:240030494:A:T
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.240030495A>T, NC_000002.11:g.240969912A>T

Select item 148260552914.

rs1482605529 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:240029735 (GRCh38)
2:240969152 (GRCh37)
Canonical SPDI:: NC_000002.12:240029734:G:A
Gene:: OR6B2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.240029735G>A, NC_000002.11:g.240969152G>A, NG_031855.2:g.668C>T, NM_001005853.1:c.695C>T, NM_001001962.1:c.695C>T, NP_001005853.1:p.Thr232Ile

Select item 148068430415.

rs1480684304 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:240030049 (GRCh38)
2:240969466 (GRCh37)
Canonical SPDI:: NC_000002.12:240030048:G:A
Gene:: OR6B2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000016/3 (GnomAD_exomes)
HGVS:: NC_000002.12:g.240030049G>A, NC_000002.11:g.240969466G>A, NG_031855.2:g.354C>T, NM_001005853.1:c.381C>T, NM_001001962.1:c.381C>T

Select item 147987859816.

rs1479878598 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:240031080 (GRCh38)
2:240970497 (GRCh37)
Canonical SPDI:: NC_000002.12:240031079:C:G
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.240031080C>G, NC_000002.11:g.240970497C>G

Select item 147944100317.

rs1479441003 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:240029318 (GRCh38)
2:240968735 (GRCh37)
Canonical SPDI:: NC_000002.12:240029317:A:G
Gene:: OR6B2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.240029318A>G, NC_000002.11:g.240968735A>G, NG_031855.2:g.1085T>C, NM_001001962.1:c.*173T>C

Select item 147917288818.

rs1479172888 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTGGAGCCACAGAACGTGACG>- [Show Flanks]
Chromosome:: 2:240029915 (GRCh38)
2:240969332 (GRCh37)
Canonical SPDI:: NC_000002.12:240029910:GACGTTGGAGCCACAGAACGTGACG:GACG
Gene:: OR6B2 (Varview)
Functional Consequence:: inframe_deletion,coding_sequence_variant
HGVS:: NC_000002.12:g.240029915_240029935del, NC_000002.11:g.240969332_240969352del, NG_031855.2:g.472_492del, NM_001005853.1:c.499_519del, NM_001001962.1:c.499_519del, NP_001005853.1:p.Thr167_Val173del

Select item 147892580219.

rs1478925802 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:240030767 (GRCh38)
2:240970184 (GRCh37)
Canonical SPDI:: NC_000002.12:240030766:G:A
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.00004/1 (TOMMO)
HGVS:: NC_000002.12:g.240030767G>A, NC_000002.11:g.240970184G>A

Select item 147828395820.

rs1478283958 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 2:240031694 (GRCh38)
2:240971111 (GRCh37)
Canonical SPDI:: NC_000002.12:240031693:C:G,NC_000002.12:240031693:C:T
Gene:: OR6B2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00003/8 (TOPMED)
HGVS:: NC_000002.12:g.240031694C>G, NC_000002.12:g.240031694C>T, NC_000002.11:g.240971111C>G, NC_000002.11:g.240971111C>T

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