SNP Links for Gene (Select 90522) - SNP

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Links from Gene

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Select item 14913618101.

rs1491361810 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AA [Show Flanks]
Chromosome:: 19:38306202 (GRCh38)
19:38796843 (GRCh37)
Canonical SPDI:: NC_000019.10:38306202:A:AAA
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: AA=0.00004/1 (TOMMO)
HGVS:: NC_000019.10:g.38306203_38306204insAA, NC_000019.9:g.38796843_38796844insAA

Select item 14912367682.

rs1491236768 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 19:38306204 (GRCh38)
19:38796844 (GRCh37)
Canonical SPDI:: NC_000019.10:38306201:CACA:CA
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CACA=0.00008/1 (ALFA)
HGVS:: NC_000019.10:g.38306202CA[1], NC_000019.9:g.38796842CA[1]

Select item 14909435233.

rs1490943523 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:38315843 (GRCh38)
19:38806483 (GRCh37)
Canonical SPDI:: NC_000019.10:38315842:C:T
Gene:: YIF1B (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.38315843C>T, NC_000019.9:g.38806483C>T

Select item 14905903604.

rs1490590360 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:38306864 (GRCh38)
19:38797504 (GRCh37)
Canonical SPDI:: NC_000019.10:38306863:G:A
Gene:: YIF1B (Varview)
Functional Consequence:: 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_000019.10:g.38306864G>A, NC_000019.9:g.38797504G>A, NM_001031731.1:c.*22C>T

Select item 14905143275.

rs1490514327 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:38307835 (GRCh38)
19:38798475 (GRCh37)
Canonical SPDI:: NC_000019.10:38307834:G:A
Gene:: YIF1B (Varview)
Functional Consequence:: 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.38307835G>A, NC_000019.9:g.38798475G>A

Select item 14904525626.

rs1490452562 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:38316126 (GRCh38)
19:38806766 (GRCh37)
Canonical SPDI:: NC_000019.10:38316125:T:C
Gene:: YIF1B (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/2 (GnomAD)
HGVS:: NC_000019.10:g.38316126T>C, NC_000019.9:g.38806766T>C

Select item 14904375527.

rs1490437552 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:38314180 (GRCh38)
19:38804820 (GRCh37)
Canonical SPDI:: NC_000019.10:38314179:C:T
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000022/3 (GnomAD)
T=0.000045/12 (TOPMED)
HGVS:: NC_000019.10:g.38314180C>T, NC_000019.9:g.38804820C>T

Select item 14901590158.

rs1490159015 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:38312688 (GRCh38)
19:38803328 (GRCh37)
Canonical SPDI:: NC_000019.10:38312687:G:A,NC_000019.10:38312687:G:C
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000043/6 (GnomAD)
HGVS:: NC_000019.10:g.38312688G>A, NC_000019.10:g.38312688G>C, NC_000019.9:g.38803328G>A, NC_000019.9:g.38803328G>C

Select item 14901127129.

rs1490112712 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:38312360 (GRCh38)
19:38803000 (GRCh37)
Canonical SPDI:: NC_000019.10:38312359:T:A
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000008/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.38312360T>A, NC_000019.9:g.38803000T>A

Select item 148999771810.

rs1489997718 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:38314666 (GRCh38)
19:38805306 (GRCh37)
Canonical SPDI:: NC_000019.10:38314665:C:T
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000019.10:g.38314666C>T, NC_000019.9:g.38805306C>T

Select item 148994793011.

rs1489947930 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGTGCC>- [Show Flanks]
Chromosome:: 19:38313242 (GRCh38)
19:38803882 (GRCh37)
Canonical SPDI:: NC_000019.10:38313239:CCAGTGCC:CC
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CC=0.0016/7 (ALFA)
HGVS:: NC_000019.10:g.38313242_38313247del, NC_000019.9:g.38803882_38803887del

Select item 148967192012.

rs1489671920 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:38311303 (GRCh38)
19:38801943 (GRCh37)
Canonical SPDI:: NC_000019.10:38311302:A:G
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000019.10:g.38311303A>G, NC_000019.9:g.38801943A>G

Select item 148910474513.

rs1489104745 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:38305772 (GRCh38)
19:38796412 (GRCh37)
Canonical SPDI:: NC_000019.10:38305771:C:G,NC_000019.10:38305771:C:T
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.38305772C>G, NC_000019.10:g.38305772C>T, NC_000019.9:g.38796412C>G, NC_000019.9:g.38796412C>T

Select item 148905248014.

rs1489052480 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:38305816 (GRCh38)
19:38796456 (GRCh37)
Canonical SPDI:: NC_000019.10:38305815:G:A
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.38305816G>A, NC_000019.9:g.38796456G>A

Select item 148869435915.

rs1488694359 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 19:38310304 (GRCh38)
19:38800944 (GRCh37)
Canonical SPDI:: NC_000019.10:38310303:T:C,NC_000019.10:38310303:T:G
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.0537/637 (ALFA)
C=0.02007/322 (TOMMO)
G=0.2305/668 (KOREAN)
HGVS:: NC_000019.10:g.38310304T>C, NC_000019.10:g.38310304T>G, NC_000019.9:g.38800944T>C, NC_000019.9:g.38800944T>G

Select item 148855494716.

rs1488554947 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:38312876 (GRCh38)
19:38803516 (GRCh37)
Canonical SPDI:: NC_000019.10:38312875:G:A
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.38312876G>A, NC_000019.9:g.38803516G>A

Select item 148855285617.

rs1488552856 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:38312387 (GRCh38)
19:38803027 (GRCh37)
Canonical SPDI:: NC_000019.10:38312386:C:T
Gene:: YIF1B (Varview)
Functional Consequence:: intron_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_000019.10:g.38312387C>T, NC_000019.9:g.38803027C>T

Select item 148821343318.

rs1488213433 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:38315959 (GRCh38)
19:38806599 (GRCh37)
Canonical SPDI:: NC_000019.10:38315958:G:A
Gene:: YIF1B (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000019.10:g.38315959G>A, NC_000019.9:g.38806599G>A, NM_001039672.2:c.-42C>T, NM_001039673.2:c.-42C>T, NM_001145463.1:c.-42C>T

Select item 148775195619.

rs1487751956 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 19:38312952 (GRCh38)
19:38803592 (GRCh37)
Canonical SPDI:: NC_000019.10:38312951:T:A,NC_000019.10:38312951:T:C
Gene:: YIF1B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.00002/2 (GnomAD)
A=0.000035/1 (TOMMO)
T=0.5/4 (SGDP_PRJ)
HGVS:: NC_000019.10:g.38312952T>A, NC_000019.10:g.38312952T>C, NC_000019.9:g.38803592T>A, NC_000019.9:g.38803592T>C

Select item 148761971220.

rs1487619712 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:38317417 (GRCh38)
19:38808057 (GRCh37)
Canonical SPDI:: NC_000019.10:38317416:A:G
Gene:: YIF1B (Varview)
Functional Consequence:: 5_prime_UTR_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.38317417A>G, NC_000019.9:g.38808057A>G, XM_047439647.1:c.-301T>C