SNP Links for Nucleotide (Select 188528608) - SNP

Links from Nucleotide

Items: 1 to 20 of 580

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Select item 14891412771.

rs1489141277 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:97771762 (GRCh38)
10:99531519 (GRCh37)
Canonical SPDI:: NC_000010.11:97771761:C:G
Gene:: SFRP5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.97771762C>G, NC_000010.10:g.99531519C>G, NM_003015.3:c.72G>C, NP_003006.2:p.Trp24Cys

Select item 14885157362.

rs1488515736 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97771400 (GRCh38)
10:99531157 (GRCh37)
Canonical SPDI:: NC_000010.11:97771399:G:A
Gene:: SFRP5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.97771400G>A, NC_000010.10:g.99531157G>A, NM_003015.3:c.434C>T, NP_003006.2:p.Pro145Leu

Select item 14872790203.

rs1487279020 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 10:97771701 (GRCh38)
10:99531458 (GRCh37)
Canonical SPDI:: NC_000010.11:97771700:G:C,NC_000010.11:97771700:G:T
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000013/3 (GnomAD_exomes)
T=0.000071/1 (TOMMO)
HGVS:: NC_000010.11:g.97771701G>C, NC_000010.11:g.97771701G>T, NC_000010.10:g.99531458G>C, NC_000010.10:g.99531458G>T, NM_003015.3:c.133C>G, NM_003015.3:c.133C>A, NP_003006.2:p.Arg45Gly, NP_003006.2:p.Arg45Ser

Select item 14852627454.

rs1485262745 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:97771636 (GRCh38)
10:99531393 (GRCh37)
Canonical SPDI:: NC_000010.11:97771635:C:T
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.97771636C>T, NC_000010.10:g.99531393C>T, NM_003015.3:c.198G>A

Select item 14837146275.

rs1483714627 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:97771619 (GRCh38)
10:99531376 (GRCh37)
Canonical SPDI:: NC_000010.11:97771618:C:T
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.97771619C>T, NC_000010.10:g.99531376C>T, NM_003015.3:c.215G>A, NP_003006.2:p.Arg72Gln

Select item 14834325066.

rs1483432506 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 10:97767167 (GRCh38)
10:99526924 (GRCh37)
Canonical SPDI:: NC_000010.11:97767164:AGAG:AG
Gene:: SFRP5 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: AGAG=0./0 (ALFA)
-=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.97767165AG[1], NC_000010.10:g.99526922AG[1], NM_003015.3:c.*346CT[1]

Select item 14790825137.

rs1479082513 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 10:97767604 (GRCh38)
10:99527361 (GRCh37)
Canonical SPDI:: NC_000010.11:97767603:A:G,NC_000010.11:97767603:A:T
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.97767604A>G, NC_000010.11:g.97767604A>T, NC_000010.10:g.99527361A>G, NC_000010.10:g.99527361A>T, NM_003015.3:c.864T>C, NM_003015.3:c.864T>A, NP_003006.2:p.Asn288Lys

Select item 14775007518.

rs1477500751 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:97771330 (GRCh38)
10:99531087 (GRCh37)
Canonical SPDI:: NC_000010.11:97771329:C:G
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.97771330C>G, NC_000010.10:g.99531087C>G, NM_003015.3:c.504G>C

Select item 14771216169.

rs1477121616 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:97771417 (GRCh38)
10:99531174 (GRCh37)
Canonical SPDI:: NC_000010.11:97771416:C:T
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000010.11:g.97771417C>T, NC_000010.10:g.99531174C>T, NM_003015.3:c.417G>A, NP_003006.2:p.Met139Ile

Select item 147704956610.

rs1477049566 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 10:97767542 (GRCh38)
10:99527299 (GRCh37)
Canonical SPDI:: NC_000010.11:97767541:AAA:AA
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.97767544del, NC_000010.10:g.99527301del, NM_003015.3:c.926del, NP_003006.2:p.Phe309fs

Select item 147599442911.

rs1475994429 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 10:97771923 (GRCh38)
10:99531680 (GRCh37)
Canonical SPDI:: NC_000010.11:97771922:A:G,NC_000010.11:97771922:A:T
Gene:: SFRP5 (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000084/1 (ALFA)
T=0.000022/3 (GnomAD)
T=0.000023/6 (TOPMED)
G=0.000071/2 (TOMMO)
HGVS:: NC_000010.11:g.97771923A>G, NC_000010.11:g.97771923A>T, NC_000010.10:g.99531680A>G, NC_000010.10:g.99531680A>T, NM_003015.3:c.-90T>C, NM_003015.3:c.-90T>A

Select item 147483451212.

rs1474834512 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:97767160 (GRCh38)
10:99526917 (GRCh37)
Canonical SPDI:: NC_000010.11:97767159:C:T
Gene:: SFRP5 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000026/7 (TOPMED)
HGVS:: NC_000010.11:g.97767160C>T, NC_000010.10:g.99526917C>T, NM_003015.3:c.*354G>A

Select item 147241395913.

rs1472413959 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97771557 (GRCh38)
10:99531314 (GRCh37)
Canonical SPDI:: NC_000010.11:97771556:G:A
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000010.11:g.97771557G>A, NC_000010.10:g.99531314G>A, NM_003015.3:c.277C>T

Select item 147045573314.

rs1470455733 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97767565 (GRCh38)
10:99527322 (GRCh37)
Canonical SPDI:: NC_000010.11:97767564:G:A
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000010.11:g.97767565G>A, NC_000010.10:g.99527322G>A, NM_003015.3:c.903C>T

Select item 147011419915.

rs1470114199 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:97766776 (GRCh38)
10:99526533 (GRCh37)
Canonical SPDI:: NC_000010.11:97766775:A:G
Gene:: SFRP5 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000010.11:g.97766776A>G, NC_000010.10:g.99526533A>G, NM_003015.3:c.*738T>C

Select item 146862320916.

rs1468623209 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:97767161 (GRCh38)
10:99526918 (GRCh37)
Canonical SPDI:: NC_000010.11:97767160:C:T
Gene:: SFRP5 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.97767161C>T, NC_000010.10:g.99526918C>T, NM_003015.3:c.*353G>A

Select item 146654380317.

rs1466543803 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTTG>- [Show Flanks]
Chromosome:: 10:97766816 (GRCh38)
10:99526573 (GRCh37)
Canonical SPDI:: NC_000010.11:97766812:TTGGTTG:TTG
Gene:: SFRP5 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: TTG=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.97766816_97766819del, NC_000010.10:g.99526573_99526576del, NM_003015.3:c.*698_*701del

Select item 146626056118.

rs1466260561 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97771830 (GRCh38)
10:99531587 (GRCh37)
Canonical SPDI:: NC_000010.11:97771829:G:A
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00003/8 (TOPMED)
A=0.000037/5 (GnomAD)
HGVS:: NC_000010.11:g.97771830G>A, NC_000010.10:g.99531587G>A, NM_003015.3:c.4C>T, NP_003006.2:p.Arg2Trp

Select item 146583719719.

rs1465837197 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97771471 (GRCh38)
10:99531228 (GRCh37)
Canonical SPDI:: NC_000010.11:97771470:G:A
Gene:: SFRP5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.97771471G>A, NC_000010.10:g.99531228G>A, NM_003015.3:c.363C>T

Select item 146558485020.

rs1465584850 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97767465 (GRCh38)
10:99527222 (GRCh37)
Canonical SPDI:: NC_000010.11:97767464:G:A
Gene:: SFRP5 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: A=0.000006/1 (GnomAD_exomes)
A=0.000546/1 (Korea1K)
HGVS:: NC_000010.11:g.97767465G>A, NC_000010.10:g.99527222G>A, NM_003015.3:c.*49C>T

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