SNP Links for Gene (Select 91039) - SNP

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Select item 14912662471.

rs1491266247 has merged into rs144927941 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:4699167 (GRCh38)
19:4699179 (GRCh37)
Canonical SPDI:: NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4699158:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
AAAAAAAAAAAAAAAAAAAAAAAAAA=0.007143/4 (NorthernSweden)
HGVS:: NC_000019.10:g.4699167_4699183del, NC_000019.10:g.4699168_4699183del, NC_000019.10:g.4699170_4699183del, NC_000019.10:g.4699171_4699183del, NC_000019.10:g.4699172_4699183del, NC_000019.10:g.4699173_4699183del, NC_000019.10:g.4699174_4699183del, NC_000019.10:g.4699175_4699183del, NC_000019.10:g.4699176_4699183del, NC_000019.10:g.4699177_4699183del, NC_000019.10:g.4699178_4699183del, NC_000019.10:g.4699179_4699183del, NC_000019.10:g.4699180_4699183del, NC_000019.10:g.4699181_4699183del, NC_000019.10:g.4699182_4699183del, NC_000019.10:g.4699183del, NC_000019.10:g.4699183dup, NC_000019.10:g.4699182_4699183dup, NC_000019.10:g.4699181_4699183dup, NC_000019.10:g.4699180_4699183dup, NC_000019.10:g.4699179_4699183dup, NC_000019.10:g.4699178_4699183dup, NC_000019.10:g.4699177_4699183dup, NC_000019.10:g.4699176_4699183dup, NC_000019.10:g.4699175_4699183dup, NC_000019.10:g.4699174_4699183dup, NC_000019.10:g.4699183_4699184insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.4699183_4699184insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.4699179_4699195del, NC_000019.9:g.4699180_4699195del, NC_000019.9:g.4699182_4699195del, NC_000019.9:g.4699183_4699195del, NC_000019.9:g.4699184_4699195del, NC_000019.9:g.4699185_4699195del, NC_000019.9:g.4699186_4699195del, NC_000019.9:g.4699187_4699195del, NC_000019.9:g.4699188_4699195del, NC_000019.9:g.4699189_4699195del, NC_000019.9:g.4699190_4699195del, NC_000019.9:g.4699191_4699195del, NC_000019.9:g.4699192_4699195del, NC_000019.9:g.4699193_4699195del, NC_000019.9:g.4699194_4699195del, NC_000019.9:g.4699195del, NC_000019.9:g.4699195dup, NC_000019.9:g.4699194_4699195dup, NC_000019.9:g.4699193_4699195dup, NC_000019.9:g.4699192_4699195dup, NC_000019.9:g.4699191_4699195dup, NC_000019.9:g.4699190_4699195dup, NC_000019.9:g.4699189_4699195dup, NC_000019.9:g.4699188_4699195dup, NC_000019.9:g.4699187_4699195dup, NC_000019.9:g.4699186_4699195dup, NC_000019.9:g.4699195_4699196insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.4699195_4699196insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14912645682.

rs1491264568 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 19:4702840 (GRCh38)
19:4702853 (GRCh37)
Canonical SPDI:: NC_000019.10:4702840::A
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.00239/33 (TOMMO)
HGVS:: NC_000019.10:g.4702840_4702841insA, NC_000019.9:g.4702852_4702853insA

Select item 14911874413.

rs1491187441 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>- [Show Flanks]
Chromosome:: 19:4702843 (GRCh38)
19:4702855 (GRCh37)
Canonical SPDI:: NC_000019.10:4702839:GGGGG:GGG
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGG=0.007/83 (ALFA)
-=0.00058/8 (TOMMO)
-=0.00066/1 (Korea1K)
HGVS:: NC_000019.10:g.4702843_4702844del, NC_000019.9:g.4702855_4702856del

Select item 14911065424.

rs1491106542 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 19:4699158 (GRCh38)
19:4699170 (GRCh37)
Canonical SPDI:: NC_000019.10:4699157:CA:
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000019.10:g.4699158_4699159del, NC_000019.9:g.4699170_4699171del

Select item 14910110265.

rs1491011026 has merged into rs531015203 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:4680666 (GRCh38)
19:4680678 (GRCh37)
Canonical SPDI:: NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4680656:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: DPP9 (Varview), DPP9-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.4680666_4680674del, NC_000019.10:g.4680672_4680674del, NC_000019.10:g.4680673_4680674del, NC_000019.10:g.4680674del, NC_000019.10:g.4680674dup, NC_000019.10:g.4680673_4680674dup, NC_000019.10:g.4680672_4680674dup, NC_000019.10:g.4680671_4680674dup, NC_000019.10:g.4680670_4680674dup, NC_000019.10:g.4680669_4680674dup, NC_000019.10:g.4680661_4680674dup, NC_000019.9:g.4680678_4680686del, NC_000019.9:g.4680684_4680686del, NC_000019.9:g.4680685_4680686del, NC_000019.9:g.4680686del, NC_000019.9:g.4680686dup, NC_000019.9:g.4680685_4680686dup, NC_000019.9:g.4680684_4680686dup, NC_000019.9:g.4680683_4680686dup, NC_000019.9:g.4680682_4680686dup, NC_000019.9:g.4680681_4680686dup, NC_000019.9:g.4680673_4680686dup

Select item 14909987106.

rs1490998710 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:4701421 (GRCh38)
19:4701433 (GRCh37)
Canonical SPDI:: NC_000019.10:4701420:T:C
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.4701421T>C, NC_000019.9:g.4701433T>C

Select item 14908829827.

rs1490882982 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:4687043 (GRCh38)
19:4687055 (GRCh37)
Canonical SPDI:: NC_000019.10:4687042:G:A
Gene:: DPP9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000026/7 (TOPMED)
A=0.000043/6 (GnomAD)
HGVS:: NC_000019.10:g.4687043G>A, NC_000019.9:g.4687055G>A

Select item 14908765968.

rs1490876596 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:4719477 (GRCh38)
19:4719489 (GRCh37)
Canonical SPDI:: NC_000019.10:4719476:A:C
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.4719477A>C, NC_000019.9:g.4719489A>C

Select item 14908728979.

rs1490872897 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:4722949 (GRCh38)
19:4722961 (GRCh37)
Canonical SPDI:: NC_000019.10:4722948:G:A
Gene:: DPP9 (Varview), LOC105372250 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.4722949G>A, NC_000019.9:g.4722961G>A, XR_936274.2:n.70G>A, XR_936274.1:n.8G>A

Select item 149066454210.

rs1490664542 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:4680933 (GRCh38)
19:4680945 (GRCh37)
Canonical SPDI:: NC_000019.10:4680932:G:T
Gene:: DPP9 (Varview), DPP9-AS1 (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_000019.10:g.4680933G>T, NC_000019.9:g.4680945G>T

Select item 149057800611.

rs1490578006 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:4715706 (GRCh38)
19:4715718 (GRCh37)
Canonical SPDI:: NC_000019.10:4715705:C:T
Gene:: DPP9 (Varview)
Functional Consequence:: 5_prime_UTR_variant,synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000019.10:g.4715706C>T, NC_000019.9:g.4715718C>T, XM_011528405.2:c.177G>A, XM_011528405.1:c.177G>A, NM_001384627.1:c.-209G>A, NM_001384623.1:c.-73G>A, NM_001384625.1:c.-73G>A, XM_047439653.1:c.-73G>A, XM_047439652.1:c.177G>A

Select item 149050402512.

rs1490504025 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 19:4701028 (GRCh38)
19:4701040 (GRCh37)
Canonical SPDI:: NC_000019.10:4701027:A:T
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000142/2 (TOMMO)
T=0.000546/1 (Korea1K)
T=0.000684/2 (KOREAN)
HGVS:: NC_000019.10:g.4701028A>T, NC_000019.9:g.4701040A>T

Select item 149046077613.

rs1490460776 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:4687551 (GRCh38)
19:4687563 (GRCh37)
Canonical SPDI:: NC_000019.10:4687550:C:A
Gene:: DPP9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_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_000019.10:g.4687551C>A, NC_000019.9:g.4687563C>A

Select item 149042987614.

rs1490429876 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 19:4686559 (GRCh38)
19:4686571 (GRCh37)
Canonical SPDI:: NC_000019.10:4686558:A:C,NC_000019.10:4686558:A:G
Gene:: DPP9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.4686559A>C, NC_000019.10:g.4686559A>G, NC_000019.9:g.4686571A>C, NC_000019.9:g.4686571A>G

Select item 149034321715.

rs1490343217 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 19:4721551 (GRCh38)
19:4721563 (GRCh37)
Canonical SPDI:: NC_000019.10:4721550:C:A,NC_000019.10:4721550:C:G,NC_000019.10:4721550:C:T
Gene:: DPP9 (Varview), LOC105372250 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.4721551C>A, NC_000019.10:g.4721551C>G, NC_000019.10:g.4721551C>T, NC_000019.9:g.4721563C>A, NC_000019.9:g.4721563C>G, NC_000019.9:g.4721563C>T

Select item 149032911116.

rs1490329111 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:4714277 (GRCh38)
19:4714289 (GRCh37)
Canonical SPDI:: NC_000019.10:4714276:G:T
Gene:: DPP9 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.4714277G>T, NC_000019.9:g.4714289G>T, NM_139159.5:c.117C>A, NM_139159.4:c.117C>A, XM_011528405.2:c.279C>A, XM_011528405.1:c.279C>A, NR_158699.2:n.374C>A, NR_158699.1:n.374C>A, NM_001365987.2:c.117C>A, NM_001365987.1:c.117C>A, NM_001384627.1:c.30C>A, NR_169286.1:n.484C>A, NM_001384626.1:c.30C>A, NM_001384623.1:c.30C>A, NM_001384624.1:c.30C>A, NM_001384612.1:c.117C>A, NR_169283.1:n.374C>A, NM_001384621.1:c.117C>A, NM_001384625.1:c.30C>A, NM_001384629.1:c.117C>A, XM_047439653.1:c.30C>A, NM_001384617.1:c.117C>A, NM_001384618.1:c.117C>A, NM_001384628.1:c.117C>A, NM_001384619.1:c.117C>A, NR_169291.1:n.374C>A, NM_001384620.1:c.117C>A, NM_001384615.1:c.117C>A, NR_169287.1:n.484C>A, NM_001384622.1:c.117C>A, NR_169290.1:n.374C>A, NR_169289.1:n.374C>A, NR_169284.1:n.374C>A, NM_001384613.1:c.117C>A, NM_001384611.1:c.117C>A, NM_001384630.1:c.117C>A, NR_169285.1:n.374C>A, NM_001384614.1:c.117C>A, NM_001384631.1:c.117C>A, XM_047439652.1:c.279C>A, NM_001384632.1:c.30C>A, NM_001384616.1:c.117C>A, NM_001384633.1:c.30C>A, NR_169288.1:n.484C>A, NM_001384634.1:c.117C>A, NR_169292.1:n.374C>A, NM_001384636.1:c.117C>A, NM_001384637.1:c.117C>A, NM_001384638.1:c.117C>A, NM_001384635.1:c.117C>A, XM_047439654.1:c.117C>A, NP_631898.3:p.Asp39Glu, XP_011526707.1:p.Asp93Glu, NP_001352916.1:p.Asp39Glu, NP_001371556.1:p.Asp10Glu, NP_001371555.1:p.Asp10Glu, NP_001371552.1:p.Asp10Glu, NP_001371553.1:p.Asp10Glu, NP_001371541.1:p.Asp39Glu, NP_001371550.1:p.Asp39Glu, NP_001371554.1:p.Asp10Glu, NP_001371558.1:p.Asp39Glu, XP_047295609.1:p.Asp10Glu, NP_001371546.1:p.Asp39Glu, NP_001371547.1:p.Asp39Glu, NP_001371557.1:p.Asp39Glu, NP_001371548.1:p.Asp39Glu, NP_001371549.1:p.Asp39Glu, NP_001371544.1:p.Asp39Glu, NP_001371551.1:p.Asp39Glu, NP_001371542.1:p.Asp39Glu, NP_001371540.1:p.Asp39Glu, NP_001371559.1:p.Asp39Glu, NP_001371543.1:p.Asp39Glu, NP_001371560.1:p.Asp39Glu, XP_047295608.1:p.Asp93Glu, NP_001371561.1:p.Asp10Glu, NP_001371545.1:p.Asp39Glu, NP_001371562.1:p.Asp10Glu, NP_001371563.1:p.Asp39Glu, NP_001371565.1:p.Asp39Glu, NP_001371566.1:p.Asp39Glu, NP_001371567.1:p.Asp39Glu, NP_001371564.1:p.Asp39Glu, XP_047295610.1:p.Asp39Glu

Select item 149024484217.

rs1490244842 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 19:4698091 (GRCh38)
19:4698103 (GRCh37)
Canonical SPDI:: NC_000019.10:4698090:GGG:GG
Gene:: DPP9 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000019.10:g.4698093del, NC_000019.9:g.4698105del

Select item 149022424618.

rs1490224246 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:4693430 (GRCh38)
19:4693442 (GRCh37)
Canonical SPDI:: NC_000019.10:4693429:C:T
Gene:: DPP9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.4693430C>T, NC_000019.9:g.4693442C>T

Select item 149014436819.

rs1490144368 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:4679682 (GRCh38)
19:4679694 (GRCh37)
Canonical SPDI:: NC_000019.10:4679681:C:G,NC_000019.10:4679681:C:T
Gene:: DPP9 (Varview), DPP9-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.4679682C>G, NC_000019.10:g.4679682C>T, NC_000019.9:g.4679694C>G, NC_000019.9:g.4679694C>T

Select item 149013923320.

rs1490139233 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGCCTTACTCATTGGGCAGC [Show Flanks]
Chromosome:: 19:4682687 (GRCh38)
19:4682700 (GRCh37)
Canonical SPDI:: NC_000019.10:4682687:GGCCTTACTCATTGGGCAGC:GGCCTTACTCATTGGGCAGCGGCCTTACTCATTGGGCAGC
Gene:: DPP9 (Varview), DPP9-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_transcript_variant,coding_sequence_variant,splice_donor_variant,intron_variant
HGVS:: NC_000019.10:g.4682688_4682707dup, NC_000019.9:g.4682700_4682719dup

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