SNP Links for Nucleotide (Select 262205443) - SNP

Links from Nucleotide

Items: 1 to 20 of 21

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Select item 14534497701.

rs1453449770 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:62824037 (GRCh38)
15:63116236 (GRCh37)
Canonical SPDI:: NC_000015.10:62824036:T:C
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000015.10:g.62824037T>C, NC_000015.9:g.63116236T>C, NG_033932.1:g.181727T>C, NR_029709.1:n.81T>C

Select item 14006971782.

rs1400697178 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:62823958 (GRCh38)
15:63116157 (GRCh37)
Canonical SPDI:: NC_000015.10:62823957:G:A
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
HGVS:: NC_000015.10:g.62823958G>A, NC_000015.9:g.63116157G>A, NG_033932.1:g.181648G>A, NR_029709.1:n.2G>A

Select item 13699264023.

rs1369926402 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:62823991 (GRCh38)
15:63116190 (GRCh37)
Canonical SPDI:: NC_000015.10:62823990:G:A
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.62823991G>A, NC_000015.9:g.63116190G>A, NG_033932.1:g.181681G>A, NR_029709.1:n.35G>A

Select item 13674785284.

rs1367478528 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:62824008 (GRCh38)
15:63116207 (GRCh37)
Canonical SPDI:: NC_000015.10:62824007:C:T
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.62824008C>T, NC_000015.9:g.63116207C>T, NG_033932.1:g.181698C>T, NR_029709.1:n.52C>T

Select item 13500002995.

rs1350000299 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:62823972 (GRCh38)
15:63116171 (GRCh37)
Canonical SPDI:: NC_000015.10:62823971:G:A
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.62823972G>A, NC_000015.9:g.63116171G>A, NG_033932.1:g.181662G>A, NR_029709.1:n.16G>A

Select item 13295608136.

rs1329560813 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:62823967 (GRCh38)
15:63116166 (GRCh37)
Canonical SPDI:: NC_000015.10:62823966:T:C
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.62823967T>C, NC_000015.9:g.63116166T>C, NG_033932.1:g.181657T>C, NR_029709.1:n.11T>C

Select item 13170104487.

rs1317010448 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:62823963 (GRCh38)
15:63116162 (GRCh37)
Canonical SPDI:: NC_000015.10:62823962:C:A,NC_000015.10:62823962:C:T
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
HGVS:: NC_000015.10:g.62823963C>A, NC_000015.10:g.62823963C>T, NC_000015.9:g.63116162C>A, NC_000015.9:g.63116162C>T, NG_033932.1:g.181653C>A, NG_033932.1:g.181653C>T, NR_029709.1:n.7C>A, NR_029709.1:n.7C>T

Select item 13112981478.

rs1311298147 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:62824010 (GRCh38)
15:63116209 (GRCh37)
Canonical SPDI:: NC_000015.10:62824009:A:G
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
G=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000015.10:g.62824010A>G, NC_000015.9:g.63116209A>G, NG_033932.1:g.181700A>G, NR_029709.1:n.54A>G

Select item 13025250569.

rs1302525056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:62824005 (GRCh38)
15:63116204 (GRCh37)
Canonical SPDI:: NC_000015.10:62824004:C:T
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
HGVS:: NC_000015.10:g.62824005C>T, NC_000015.9:g.63116204C>T, NG_033932.1:g.181695C>T, NR_029709.1:n.49C>T

Select item 129064438910.

rs1290644389 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:62824031 (GRCh38)
15:63116230 (GRCh37)
Canonical SPDI:: NC_000015.10:62824030:A:G
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
HGVS:: NC_000015.10:g.62824031A>G, NC_000015.9:g.63116230A>G, NG_033932.1:g.181721A>G, NR_029709.1:n.75A>G

Select item 128130377111.

rs1281303771 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:62823976 (GRCh38)
15:63116175 (GRCh37)
Canonical SPDI:: NC_000015.10:62823975:T:C
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.62823976T>C, NC_000015.9:g.63116175T>C, NG_033932.1:g.181666T>C, NR_029709.1:n.20T>C

Select item 122889917412.

rs1228899174 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 15:62823974 (GRCh38)
15:63116173 (GRCh37)
Canonical SPDI:: NC_000015.10:62823973:T:A
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000015.10:g.62823974T>A, NC_000015.9:g.63116173T>A, NG_033932.1:g.181664T>A, NR_029709.1:n.18T>A

Select item 121200692413.

rs1212006924 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:62824040 (GRCh38)
15:63116239 (GRCh37)
Canonical SPDI:: NC_000015.10:62824039:C:T
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
HGVS:: NC_000015.10:g.62824040C>T, NC_000015.9:g.63116239C>T, NG_033932.1:g.181730C>T, NR_029709.1:n.84C>T

Select item 101870677714.

rs1018706777 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:62823984 (GRCh38)
15:63116183 (GRCh37)
Canonical SPDI:: NC_000015.10:62823983:A:G
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000015.10:g.62823984A>G, NC_000015.9:g.63116183A>G, NG_033932.1:g.181674A>G, NR_029709.1:n.28A>G

Select item 77746461315.

rs777464613 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 15:62823987 (GRCh38)
15:63116186 (GRCh37)
Canonical SPDI:: NC_000015.10:62823986:T:A,NC_000015.10:62823986:T:G
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000016/4 (GnomAD_exomes)
G=0.000031/3 (ExAC)
G=0.000034/9 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000015.10:g.62823987T>A, NC_000015.10:g.62823987T>G, NC_000015.9:g.63116186T>A, NC_000015.9:g.63116186T>G, NG_033932.1:g.181677T>A, NG_033932.1:g.181677T>G, NR_029709.1:n.31T>A, NR_029709.1:n.31T>G

Select item 77104395516.

rs771043955 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 15:62824015 (GRCh38)
15:63116214 (GRCh37)
Canonical SPDI:: NC_000015.10:62824014:T:A,NC_000015.10:62824014:T:C
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
C=0.000011/1 (ExAC)
HGVS:: NC_000015.10:g.62824015T>A, NC_000015.10:g.62824015T>C, NC_000015.9:g.63116214T>A, NC_000015.9:g.63116214T>C, NG_033932.1:g.181705T>A, NG_033932.1:g.181705T>C, NR_029709.1:n.59T>A, NR_029709.1:n.59T>C

Select item 76674287217.

rs766742872 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTT>- [Show Flanks]
Chromosome:: 15:62823994 (GRCh38)
15:63116193 (GRCh37)
Canonical SPDI:: NC_000015.10:62823990:GTTGTT:GTT
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTTGTT=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000004/1 (TOPMED)
-=0.00001/1 (ExAC)
HGVS:: NC_000015.10:g.62823991GTT[1], NC_000015.9:g.63116190GTT[1], NG_033932.1:g.181681GTT[1], NR_029709.1:n.35GTT[1]

Select item 75586686818.

rs755866868 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:62823986 (GRCh38)
15:63116185 (GRCh37)
Canonical SPDI:: NC_000015.10:62823985:A:G
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: A=0./0 (SGDP_PRJ)
G=0.000004/1 (GnomAD_exomes)
G=0.00001/1 (ExAC)
HGVS:: NC_000015.10:g.62823986A>G, NC_000015.9:g.63116185A>G, NG_033932.1:g.181676A>G, NR_029709.1:n.30A>G

Select item 74920464519.

rs749204645 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 15:62823998 (GRCh38)
15:63116197 (GRCh37)
Canonical SPDI:: NC_000015.10:62823997:T:A
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.000008/2 (GnomAD_exomes)
A=0.000021/2 (ExAC)
HGVS:: NC_000015.10:g.62823998T>A, NC_000015.9:g.63116197T>A, NG_033932.1:g.181688T>A, NR_029709.1:n.42T>A

Select item 74544012720.

rs745440127 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:62824041 (GRCh38)
15:63116240 (GRCh37)
Canonical SPDI:: NC_000015.10:62824040:C:G,NC_000015.10:62824040:C:T
Gene:: TLN2 (Varview), MIR190A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
G=0.000011/1 (ExAC)
G=0.000017/4 (GnomAD_exomes)
HGVS:: NC_000015.10:g.62824041C>G, NC_000015.10:g.62824041C>T, NC_000015.9:g.63116240C>G, NC_000015.9:g.63116240C>T, NG_033932.1:g.181731C>G, NG_033932.1:g.181731C>T, NR_029709.1:n.85C>G, NR_029709.1:n.85C>T

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