SNP Links for Nucleotide (Select 683524113) - SNP

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Links from Nucleotide

Items: 1 to 20 of 76

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Select item 14904345441.

rs1490434544 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248699067 (GRCh38)
1:248862368 (GRCh37)
Canonical SPDI:: NC_000001.11:248699066:C:T
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.012/22 (Korea1K)
HGVS:: NC_000001.11:g.248699067C>T, NC_000001.10:g.248862368C>T, XM_047420643.1:c.-356G>A, NR_125950.1:n.355C>T

Select item 14797306772.

rs1479730677 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:248698961 (GRCh38)
1:248862262 (GRCh37)
Canonical SPDI:: NC_000001.11:248698960:G:A
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.248698961G>A, NC_000001.10:g.248862262G>A, XM_047420643.1:c.-250C>T, NR_125950.1:n.249G>A

Select item 14670994563.

rs1467099456 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:248697130 (GRCh38)
1:248860431 (GRCh37)
Canonical SPDI:: NC_000001.11:248697129:G:C
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,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_000001.11:g.248697130G>C, NC_000001.10:g.248860431G>C, NR_125950.1:n.69G>C

Select item 14557681584.

rs1455768158 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:248698952 (GRCh38)
1:248862253 (GRCh37)
Canonical SPDI:: NC_000001.11:248698951:A:C
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.248698952A>C, NC_000001.10:g.248862253A>C, XM_047420643.1:c.-241T>G, NR_125950.1:n.240A>C

Select item 14455667095.

rs1445566709 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:248699003 (GRCh38)
1:248862304 (GRCh37)
Canonical SPDI:: NC_000001.11:248699002:C:G
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.248699003C>G, NC_000001.10:g.248862304C>G, XM_047420643.1:c.-292G>C, NR_125950.1:n.291C>G

Select item 14435900336.

rs1443590033 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:248699022 (GRCh38)
1:248862323 (GRCh37)
Canonical SPDI:: NC_000001.11:248699021:T:C
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.248699022T>C, NC_000001.10:g.248862323T>C, XM_047420643.1:c.-311A>G, NR_125950.1:n.310T>C

Select item 14229060687.

rs1422906068 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:248697169 (GRCh38)
1:248860470 (GRCh37)
Canonical SPDI:: NC_000001.11:248697168:A:T
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000084/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.248697169A>T, NC_000001.10:g.248860470A>T, NR_125950.1:n.108A>T

Select item 14174902948.

rs1417490294 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:248699073 (GRCh38)
1:248862374 (GRCh37)
Canonical SPDI:: NC_000001.11:248699072:A:T
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.248699073A>T, NC_000001.10:g.248862374A>T, XM_047420643.1:c.-362T>A, NR_125950.1:n.361A>T

Select item 14109530279.

rs1410953027 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248698925 (GRCh38)
1:248862226 (GRCh37)
Canonical SPDI:: NC_000001.11:248698924:C:T
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.248698925C>T, NC_000001.10:g.248862226C>T, XM_047420643.1:c.-214G>A, NR_125950.1:n.213C>T

Select item 140688390610.

rs1406883906 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:248698920 (GRCh38)
1:248862221 (GRCh37)
Canonical SPDI:: NC_000001.11:248698919:G:A
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000054/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
A=0.000035/1 (TOMMO)
A=0.000223/1 (Estonian)
HGVS:: NC_000001.11:g.248698920G>A, NC_000001.10:g.248862221G>A, XM_047420643.1:c.-209C>T, NR_125950.1:n.208G>A

Select item 140483064511.

rs1404830645 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248697104 (GRCh38)
1:248860405 (GRCh37)
Canonical SPDI:: NC_000001.11:248697103:C:T
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_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_000001.11:g.248697104C>T, NC_000001.10:g.248860405C>T, NR_125950.1:n.43C>T

Select item 139605280112.

rs1396052801 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:248699063 (GRCh38)
1:248862364 (GRCh37)
Canonical SPDI:: NC_000001.11:248699062:G:A
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.248699063G>A, NC_000001.10:g.248862364G>A, XM_047420643.1:c.-352C>T, NR_125950.1:n.351G>A

Select item 138840170613.

rs1388401706 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248698864 (GRCh38)
1:248862165 (GRCh37)
Canonical SPDI:: NC_000001.11:248698863:C:T
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_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=0.000156/1 (1000Genomes)
HGVS:: NC_000001.11:g.248698864C>T, NC_000001.10:g.248862165C>T, NM_001004734.3:c.-153G>A, XM_047420643.1:c.-153G>A, NR_125950.1:n.152C>T

Select item 138687062714.

rs1386870627 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:248697203 (GRCh38)
1:248860504 (GRCh37)
Canonical SPDI:: NC_000001.11:248697202:C:G
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
HGVS:: NC_000001.11:g.248697203C>G, NC_000001.10:g.248860504C>G, NR_125950.1:n.142C>G

Select item 138262110515.

rs1382621105 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:248697147 (GRCh38)
1:248860448 (GRCh37)
Canonical SPDI:: NC_000001.11:248697146:C:G
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000038/10 (TOPMED)
G=0.00005/7 (GnomAD)
HGVS:: NC_000001.11:g.248697147C>G, NC_000001.10:g.248860448C>G, NR_125950.1:n.86C>G

Select item 137446099716.

rs1374460997 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:248697085 (GRCh38)
1:248860386 (GRCh37)
Canonical SPDI:: NC_000001.11:248697084:G:C
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.248697085G>C, NC_000001.10:g.248860386G>C, NR_125950.1:n.24G>C

Select item 137266186417.

rs1372661864 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:248698907 (GRCh38)
1:248862208 (GRCh37)
Canonical SPDI:: NC_000001.11:248698906:T:A
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.248698907T>A, NC_000001.10:g.248862208T>A, XM_047420643.1:c.-196A>T, NR_125950.1:n.195T>A

Select item 136248248818.

rs1362482488 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:248698889 (GRCh38)
1:248862190 (GRCh37)
Canonical SPDI:: NC_000001.11:248698888:G:A
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_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_000001.11:g.248698889G>A, NC_000001.10:g.248862190G>A, NM_001004734.3:c.-178C>T, XM_047420643.1:c.-178C>T, NR_125950.1:n.177G>A

Select item 135919944819.

rs1359199448 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:248697131 (GRCh38)
1:248860432 (GRCh37)
Canonical SPDI:: NC_000001.11:248697130:G:A
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: genic_upstream_transcript_variant,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_000001.11:g.248697131G>A, NC_000001.10:g.248860432G>A, NR_125950.1:n.70G>A

Select item 134986214920.

rs1349862149 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:248699097 (GRCh38)
1:248862398 (GRCh37)
Canonical SPDI:: NC_000001.11:248699096:A:T
Gene:: OR14I1 (Varview), LYPD9P (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,5_prime_UTR_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_000001.11:g.248699097A>T, NC_000001.10:g.248862398A>T, XM_047420643.1:c.-386T>A, NR_125950.1:n.385A>T