SNP Links for Gene (Select 408029) - SNP

Links from Gene

Items: 1 to 20 of 2463

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Select item 14905321981.

rs1490532198 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:131802520 (GRCh38)
2:132560093 (GRCh37)
Canonical SPDI:: NC_000002.12:131802519:A:G
Gene:: CDRT15P3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.131802520A>G, NC_000002.11:g.132560093A>G, NT_187528.1:g.106512A>G

Select item 14904922342.

rs1490492234 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 2:131796737 (GRCh38)
2:132554310 (GRCh37)
Canonical SPDI:: NC_000002.12:131796736:T:A
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.131796737T>A, NC_000002.11:g.132554310T>A, NT_187528.1:g.100730T>A

Select item 14904408193.

rs1490440819 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:131797360 (GRCh38)
2:132554933 (GRCh37)
Canonical SPDI:: NC_000002.12:131797359:C:T
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.131797360C>T, NC_000002.11:g.132554933C>T, NT_187528.1:g.101353C>T

Select item 14901149454.

rs1490114945 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:131797987 (GRCh38)
2:132555560 (GRCh37)
Canonical SPDI:: NC_000002.12:131797986:A:G
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000002.12:g.131797987A>G, NC_000002.11:g.132555560A>G, NT_187528.1:g.101980A>G

Select item 14893137425.

rs1489313742 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131797820 (GRCh38)
2:132555393 (GRCh37)
Canonical SPDI:: NC_000002.12:131797819:G:A
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.131797820G>A, NC_000002.11:g.132555393G>A, NT_187528.1:g.101813G>A

Select item 14892890166.

rs1489289016 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:131801029 (GRCh38)
2:132558602 (GRCh37)
Canonical SPDI:: NC_000002.12:131801028:T:C
Gene:: CDRT15P3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.131801029T>C, NC_000002.11:g.132558602T>C, NT_187528.1:g.105021T>C, NM_214461.2:c.-92A>G, NR_161366.1:n.402A>G, NM_214461.1:c.-92A>G

Select item 14889965557.

rs1488996555 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACAG>- [Show Flanks]
Chromosome:: 2:131801099 (GRCh38)
2:132558672 (GRCh37)
Canonical SPDI:: NC_000002.12:131801096:AGACAG:AG
Gene:: CDRT15P3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.131801099_131801102del, NC_000002.11:g.132558672_132558675del, NT_187528.1:g.105091_105094del, NM_214461.2:c.-163_-160del, NR_161366.1:n.331_334del, NM_214461.1:c.-163_-160del

Select item 14887945938.

rs1488794593 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:131796045 (GRCh38)
2:132553618 (GRCh37)
Canonical SPDI:: NC_000002.12:131796044:G:A,NC_000002.12:131796044:G:C
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.00004/1 (TOMMO)
HGVS:: NC_000002.12:g.131796045G>A, NC_000002.12:g.131796045G>C, NC_000002.11:g.132553618G>A, NC_000002.11:g.132553618G>C, NT_187528.1:g.100038G>A, NT_187528.1:g.100038G>C

Select item 14885865999.

rs1488586599 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131798070 (GRCh38)
2:132555643 (GRCh37)
Canonical SPDI:: NC_000002.12:131798069:G:A
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/1 (GnomAD)
HGVS:: NC_000002.12:g.131798070G>A, NC_000002.11:g.132555643G>A, NT_187528.1:g.102063G>A

Select item 148858564810.

rs1488585648 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131799595 (GRCh38)
2:132557168 (GRCh37)
Canonical SPDI:: NC_000002.12:131799594:G:A
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: A=0.000009/1 (GnomAD)
HGVS:: NC_000002.12:g.131799595G>A, NC_000002.11:g.132557168G>A, NT_187528.1:g.103587G>A

Select item 148855658711.

rs1488556587 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 2:131798745 (GRCh38)
2:132556318 (GRCh37)
Canonical SPDI:: NC_000002.12:131798744:A:
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_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.131798745del, NC_000002.11:g.132556318del, NT_187528.1:g.102738del

Select item 148836108912.

rs1488361089 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:131801695 (GRCh38)
2:132559268 (GRCh37)
Canonical SPDI:: NC_000002.12:131801694:C:T
Gene:: CDRT15P3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000002.12:g.131801695C>T, NC_000002.11:g.132559268C>T, NT_187528.1:g.105687C>T

Select item 148833991713.

rs1488339917 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131801704 (GRCh38)
2:132559277 (GRCh37)
Canonical SPDI:: NC_000002.12:131801703:G:A
Gene:: CDRT15P3 (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=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.131801704G>A, NC_000002.11:g.132559277G>A, NT_187528.1:g.105696G>A

Select item 148831186314.

rs1488311863 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 2:131801483 (GRCh38)
2:132559056 (GRCh37)
Canonical SPDI:: NC_000002.12:131801482:C:A,NC_000002.12:131801482:C:G
Gene:: CDRT15P3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000002.12:g.131801483C>A, NC_000002.12:g.131801483C>G, NC_000002.11:g.132559056C>A, NC_000002.11:g.132559056C>G, NT_187528.1:g.105475C>A, NT_187528.1:g.105475C>G, NM_214461.2:c.-315G>T, NM_214461.2:c.-315G>C, NR_161366.1:n.179G>T, NR_161366.1:n.179G>C, NM_214461.1:c.-315G>T, NM_214461.1:c.-315G>C

Select item 148827660315.

rs1488276603 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:131802858 (GRCh38)
2:132560431 (GRCh37)
Canonical SPDI:: NC_000002.12:131802857:C:G
Gene:: CDRT15P3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000002.12:g.131802858C>G, NC_000002.11:g.132560431C>G, NT_187528.1:g.106850C>G

Select item 148792749716.

rs1487927497 [Homo sapiens]

Variant type:: SNV:
Alleles:: CC>-
Chromosome:: no mapping
Canonical SPDI:

Select item 148787815117.

rs1487878151 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:131796859 (GRCh38)
2:132554432 (GRCh37)
Canonical SPDI:: NC_000002.12:131796858:G:C
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.131796859G>C, NC_000002.11:g.132554432G>C, NT_187528.1:g.100852G>C

Select item 148758575718.

rs1487585757 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131796396 (GRCh38)
2:132553969 (GRCh37)
Canonical SPDI:: NC_000002.12:131796395:G:A
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000002.12:g.131796396G>A, NC_000002.11:g.132553969G>A, NT_187528.1:g.100389G>A

Select item 148748624319.

rs1487486243 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:131797066 (GRCh38)
2:132554639 (GRCh37)
Canonical SPDI:: NC_000002.12:131797065:G:T
Gene:: CDRT15P3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000008/1 (GnomAD)
HGVS:: NC_000002.12:g.131797066G>T, NC_000002.11:g.132554639G>T, NT_187528.1:g.101059G>T

Select item 148726300720.

rs1487263007 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131802004 (GRCh38)
2:132559577 (GRCh37)
Canonical SPDI:: NC_000002.12:131802003:G:A
Gene:: CDRT15P3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.131802004G>A, NC_000002.11:g.132559577G>A, NT_187528.1:g.105996G>A

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