SNP Links for Nucleotide (Select 654825356) - SNP

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Links from Nucleotide

Items: 1 to 20 of 129

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Select item 14759186851.

rs1475918685 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:139978760 (GRCh38)
6:140299897 (GRCh37)
Canonical SPDI:: NC_000006.12:139978759:A:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.139978760A>G, NC_000006.11:g.140299897A>G, NR_121624.1:n.383T>C

Select item 14744739602.

rs1474473960 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:139991073 (GRCh38)
6:140312210 (GRCh37)
Canonical SPDI:: NC_000006.12:139991072:T:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.139991073T>C, NC_000006.11:g.140312210T>C, NR_121624.1:n.189A>G

Select item 14738729103.

rs1473872910 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 6:139978685 (GRCh38)
6:140299822 (GRCh37)
Canonical SPDI:: NC_000006.12:139978684:A:G,NC_000006.12:139978684:A:T
Gene:: LINC02941 (Varview), LOC103352541 (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)
G=0.000014/2 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000006.12:g.139978685A>G, NC_000006.12:g.139978685A>T, NC_000006.11:g.140299822A>G, NC_000006.11:g.140299822A>T, NR_121624.1:n.458T>C, NR_121624.1:n.458T>A

Select item 14699902344.

rs1469990234 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:139978871 (GRCh38)
6:140300008 (GRCh37)
Canonical SPDI:: NC_000006.12:139978870:C:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000006.12:g.139978871C>T, NC_000006.11:g.140300008C>T, NR_121624.1:n.272G>A

Select item 14482269535.

rs1448226953 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 6:139978825 (GRCh38)
6:140299962 (GRCh37)
Canonical SPDI:: NC_000006.12:139978824:A:G,NC_000006.12:139978824:A:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.139978825A>G, NC_000006.12:g.139978825A>T, NC_000006.11:g.140299962A>G, NC_000006.11:g.140299962A>T, NR_121624.1:n.318T>C, NR_121624.1:n.318T>A

Select item 14413669296.

rs1441366929 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:139978714 (GRCh38)
6:140299851 (GRCh37)
Canonical SPDI:: NC_000006.12:139978713:G:A
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_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_000006.12:g.139978714G>A, NC_000006.11:g.140299851G>A, NR_121624.1:n.429C>T

Select item 14378208227.

rs1437820822 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:139991206 (GRCh38)
6:140312343 (GRCh37)
Canonical SPDI:: NC_000006.12:139991205:T:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.139991206T>C, NC_000006.11:g.140312343T>C, NR_121624.1:n.56A>G

Select item 14258227058.

rs1425822705 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:139991063 (GRCh38)
6:140312200 (GRCh37)
Canonical SPDI:: NC_000006.12:139991062:C:A
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000006.12:g.139991063C>A, NC_000006.11:g.140312200C>A, NR_121624.1:n.199G>T

Select item 14179106579.

rs1417910657 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 6:139978762 (GRCh38)
6:140299900 (GRCh37)
Canonical SPDI:: NC_000006.12:139978762:TTT:TTTT
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.139978765dup, NC_000006.11:g.140299902dup, NR_121624.1:n.380dup

Select item 140820027510.

rs1408200275 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:139991142 (GRCh38)
6:140312279 (GRCh37)
Canonical SPDI:: NC_000006.12:139991141:C:A
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_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_000006.12:g.139991142C>A, NC_000006.11:g.140312279C>A, NR_121624.1:n.120G>T

Select item 140645965311.

rs1406459653 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:139978857 (GRCh38)
6:140299994 (GRCh37)
Canonical SPDI:: NC_000006.12:139978856:T:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.139978857T>C, NC_000006.11:g.140299994T>C, NR_121624.1:n.286A>G

Select item 137961357112.

rs1379613571 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:139991246 (GRCh38)
6:140312383 (GRCh37)
Canonical SPDI:: NC_000006.12:139991245:C:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.139991246C>G, NC_000006.11:g.140312383C>G, NR_121624.1:n.16G>C

Select item 137081218413.

rs1370812184 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 6:139978860 (GRCh38)
6:140299997 (GRCh37)
Canonical SPDI:: NC_000006.12:139978859:C:A,NC_000006.12:139978859:C:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.139978860C>A, NC_000006.12:g.139978860C>G, NC_000006.11:g.140299997C>A, NC_000006.11:g.140299997C>G, NR_121624.1:n.283G>T, NR_121624.1:n.283G>C

Select item 137000921114.

rs1370009211 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:139991143 (GRCh38)
6:140312280 (GRCh37)
Canonical SPDI:: NC_000006.12:139991142:A:T
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.139991143A>T, NC_000006.11:g.140312280A>T, NR_121624.1:n.119T>A

Select item 136992092915.

rs1369920929 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:139978829 (GRCh38)
6:140299966 (GRCh37)
Canonical SPDI:: NC_000006.12:139978828:T:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.139978829T>C, NC_000006.11:g.140299966T>C, NR_121624.1:n.314A>G

Select item 135960924316.

rs1359609243 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:139991138 (GRCh38)
6:140312275 (GRCh37)
Canonical SPDI:: NC_000006.12:139991137:A:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.139991138A>G, NC_000006.11:g.140312275A>G, NR_121624.1:n.124T>C

Select item 135774944717.

rs1357749447 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:139991003 (GRCh38)
6:140312140 (GRCh37)
Canonical SPDI:: NC_000006.12:139991002:A:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.139991003A>G, NC_000006.11:g.140312140A>G, NR_121624.1:n.259T>C

Select item 135740678318.

rs1357406783 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 6:139978700 (GRCh38)
6:140299837 (GRCh37)
Canonical SPDI:: NC_000006.12:139978699:T:C,NC_000006.12:139978699:T:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000034/9 (TOPMED)
C=0.000035/1 (TOMMO)
C=0.000342/1 (KOREAN)
HGVS:: NC_000006.12:g.139978700T>C, NC_000006.12:g.139978700T>G, NC_000006.11:g.140299837T>C, NC_000006.11:g.140299837T>G, NR_121624.1:n.443A>G, NR_121624.1:n.443A>C

Select item 135260645119.

rs1352606451 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 6:139978731 (GRCh38)
6:140299868 (GRCh37)
Canonical SPDI:: NC_000006.12:139978730:T:C,NC_000006.12:139978730:T:G
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.139978731T>C, NC_000006.12:g.139978731T>G, NC_000006.11:g.140299868T>C, NC_000006.11:g.140299868T>G, NR_121624.1:n.412A>G, NR_121624.1:n.412A>C

Select item 133710938520.

rs1337109385 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 6:139978797 (GRCh38)
6:140299934 (GRCh37)
Canonical SPDI:: NC_000006.12:139978796:T:A,NC_000006.12:139978796:T:C
Gene:: LINC02941 (Varview), LOC103352541 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000006.12:g.139978797T>A, NC_000006.12:g.139978797T>C, NC_000006.11:g.140299934T>A, NC_000006.11:g.140299934T>C, NR_121624.1:n.346A>T, NR_121624.1:n.346A>G