SNP Links for Nucleotide (Select 1209185318) - SNP

Links from Nucleotide

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Select item 14872577281.

rs1487257728 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:46275311 (GRCh38)
17:44352677 (GRCh37)
Canonical SPDI:: NC_000017.11:46275310:G:T
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.46275311G>T, NC_000017.10:g.44352677G>T, NT_167251.2:g.511304C>A, NT_167251.1:g.513297C>A, NT_187663.1:g.977700G>T, NM_001103154.2:c.*129C>A

Select item 14844995362.

rs1484499536 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:46352827 (GRCh38)
17:44430193 (GRCh37)
Canonical SPDI:: NC_000017.11:46352826:G:A
Gene:: ARL17B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.00003/3 (GnomAD)
HGVS:: NC_000017.11:g.46352827G>A, NC_000017.10:g.44430193G>A, NT_167251.2:g.398510C>T, NT_167251.1:g.400503C>T, NM_001039083.5:c.252C>T, NM_001039083.4:c.252C>T, NM_001039083.3:c.252C>T, XR_951553.4:n.457C>T, XR_951553.3:n.475C>T, XR_951553.2:n.469C>T, XR_951553.1:n.773C>T, XM_006725284.4:c.252C>T, XM_006725284.3:c.252C>T, XM_006725284.2:c.252C>T, XM_006725284.1:c.252C>T, XM_011546390.4:c.252C>T, XM_011546390.3:c.252C>T, XM_011546390.2:c.252C>T, XM_011546390.1:c.252C>T, XM_006725288.4:c.252C>T, XM_006725288.3:c.252C>T, XM_006725288.2:c.252C>T, XM_006725288.1:c.252C>T, XM_011546389.3:c.252C>T, XM_011546389.2:c.252C>T, XM_011546389.1:c.252C>T, XR_951556.3:n.457C>T, XR_951556.2:n.469C>T, XR_951556.1:n.773C>T, XR_951554.3:n.457C>T, XR_951554.2:n.469C>T, XR_951554.1:n.773C>T, XR_951557.3:n.457C>T, XR_951557.2:n.469C>T, XR_951557.1:n.773C>T, XM_011546387.3:c.252C>T, XM_011546387.2:c.252C>T, XM_011546387.1:c.252C>T, XR_951555.3:n.457C>T, XR_951555.2:n.469C>T, XR_951555.1:n.773C>T, XM_011546391.3:c.252C>T, XM_011546391.2:c.252C>T, XM_011546391.1:c.252C>T, NM_001352769.1:c.252C>T, NM_001103154.2:c.252C>T, NM_001103154.1:c.252C>T, XM_017030176.2:c.252C>T, XM_017030176.1:c.252C>T, XM_024452506.2:c.252C>T, XM_024452506.1:c.252C>T, NM_001363805.1:c.252C>T, NM_001330240.1:c.252C>T, XM_024452507.2:c.252C>T, XM_024452507.1:c.252C>T, XR_007068576.1:n.454C>T, XM_047442814.1:c.252C>T, XM_047442815.1:c.252C>T

Select item 14821065563.

rs1482106556 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:46274751 (GRCh38)
17:44352117 (GRCh37)
Canonical SPDI:: NC_000017.11:46274750:C:T
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.46274751C>T, NC_000017.10:g.44352117C>T, NT_167251.2:g.511860G>A, NT_167251.1:g.513853G>A, NT_187663.1:g.977140C>T, NM_001103154.2:c.*689G>A

Select item 14809219294.

rs1480921929 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:46274621 (GRCh38)
17:44351987 (GRCh37)
Canonical SPDI:: NC_000017.11:46274620:A:C
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,3_prime_UTR_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_000017.11:g.46274621A>C, NC_000017.10:g.44351987A>C, NT_167251.2:g.511990T>G, NT_167251.1:g.513983T>G, NT_187663.1:g.977010A>C, NM_001103154.2:c.*819T>G

Select item 14771786075.

rs1477178607 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:46352848 (GRCh38)
17:44430214 (GRCh37)
Canonical SPDI:: NC_000017.11:46352847:C:T
Gene:: ARL17B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000038/4 (GnomAD)
HGVS:: NC_000017.11:g.46352848C>T, NC_000017.10:g.44430214C>T, NT_167251.2:g.398489G>A, NT_167251.1:g.400482G>A, NM_001039083.5:c.231G>A, NM_001039083.4:c.231G>A, NM_001039083.3:c.231G>A, XR_951553.4:n.436G>A, XR_951553.3:n.454G>A, XR_951553.2:n.448G>A, XR_951553.1:n.752G>A, XM_006725284.4:c.231G>A, XM_006725284.3:c.231G>A, XM_006725284.2:c.231G>A, XM_006725284.1:c.231G>A, XM_011546390.4:c.231G>A, XM_011546390.3:c.231G>A, XM_011546390.2:c.231G>A, XM_011546390.1:c.231G>A, XM_006725288.4:c.231G>A, XM_006725288.3:c.231G>A, XM_006725288.2:c.231G>A, XM_006725288.1:c.231G>A, XM_011546389.3:c.231G>A, XM_011546389.2:c.231G>A, XM_011546389.1:c.231G>A, XR_951556.3:n.436G>A, XR_951556.2:n.448G>A, XR_951556.1:n.752G>A, XR_951554.3:n.436G>A, XR_951554.2:n.448G>A, XR_951554.1:n.752G>A, XR_951557.3:n.436G>A, XR_951557.2:n.448G>A, XR_951557.1:n.752G>A, XM_011546387.3:c.231G>A, XM_011546387.2:c.231G>A, XM_011546387.1:c.231G>A, XR_951555.3:n.436G>A, XR_951555.2:n.448G>A, XR_951555.1:n.752G>A, XM_011546391.3:c.231G>A, XM_011546391.2:c.231G>A, XM_011546391.1:c.231G>A, NM_001352769.1:c.231G>A, NM_001103154.2:c.231G>A, NM_001103154.1:c.231G>A, XM_017030176.2:c.231G>A, XM_017030176.1:c.231G>A, XM_024452506.2:c.231G>A, XM_024452506.1:c.231G>A, NM_001363805.1:c.231G>A, NM_001330240.1:c.231G>A, XM_024452507.2:c.231G>A, XM_024452507.1:c.231G>A, XR_007068576.1:n.433G>A, XM_047442814.1:c.231G>A, XM_047442815.1:c.231G>A

Select item 14769650776.

rs1476965077 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:46274496 (GRCh38)
17:44351862 (GRCh37)
Canonical SPDI:: NC_000017.11:46274495:T:C
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.46274496T>C, NC_000017.10:g.44351862T>C, NT_167251.2:g.512115A>G, NT_167251.1:g.514108A>G, NT_187663.1:g.976885T>C, NM_001103154.2:c.*944A>G

Select item 14762604547.

rs1476260454 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:46274887 (GRCh38)
17:44352253 (GRCh37)
Canonical SPDI:: NC_000017.11:46274886:C:T
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.46274887C>T, NC_000017.10:g.44352253C>T, NT_167251.2:g.511726G>A, NT_167251.1:g.513719G>A, NT_187663.1:g.977276C>T, NM_001103154.2:c.*553G>A

Select item 14722288188.

rs1472228818 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 17:46361701 (GRCh38)
17:44439067 (GRCh37)
Canonical SPDI:: NC_000017.11:46361700:C:A,NC_000017.11:46361700:C:T
Gene:: ARL17B (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000012/1 (GnomAD)
T=0.000255/4 (TOMMO)
HGVS:: NC_000017.11:g.46361701C>A, NC_000017.11:g.46361701C>T, NC_000017.10:g.44439067C>A, NC_000017.10:g.44439067C>T, NG_056914.1:g.99C>A, NG_056914.1:g.99C>T, NT_167251.2:g.389686G>T, NT_167251.2:g.389686G>A, NT_167251.1:g.391679G>T, NT_167251.1:g.391679G>A, NM_001039083.5:c.-43G>T, NM_001039083.5:c.-43G>A, NM_001039083.4:c.-43G>T, NM_001039083.4:c.-43G>A, NM_001039083.3:c.-43G>T, NM_001039083.3:c.-43G>A, XR_951553.4:n.163G>T, XR_951553.4:n.163G>A, XR_951553.3:n.181G>T, XR_951553.3:n.181G>A, XR_951553.2:n.175G>T, XR_951553.2:n.175G>A, XR_951553.1:n.479G>T, XR_951553.1:n.479G>A, XM_006725284.4:c.-43G>T, XM_006725284.4:c.-43G>A, XM_006725284.3:c.-43G>T, XM_006725284.3:c.-43G>A, XM_006725284.2:c.-43G>T, XM_006725284.2:c.-43G>A, XM_006725284.1:c.-43G>T, XM_006725284.1:c.-43G>A, XM_011546390.4:c.-43G>T, XM_011546390.4:c.-43G>A, XM_011546390.3:c.-43G>T, XM_011546390.3:c.-43G>A, XM_011546390.2:c.-43G>T, XM_011546390.2:c.-43G>A, XM_011546390.1:c.-43G>T, XM_011546390.1:c.-43G>A, XM_006725288.4:c.-43G>T, XM_006725288.4:c.-43G>A, XM_006725288.3:c.-43G>T, XM_006725288.3:c.-43G>A, XM_006725288.2:c.-43G>T, XM_006725288.2:c.-43G>A, XM_006725288.1:c.-43G>T, XM_006725288.1:c.-43G>A, XM_011546389.3:c.-43G>T, XM_011546389.3:c.-43G>A, XM_011546389.2:c.-43G>T, XM_011546389.2:c.-43G>A, XM_011546389.1:c.-43G>T, XM_011546389.1:c.-43G>A, XR_951556.3:n.163G>T, XR_951556.3:n.163G>A, XR_951556.2:n.175G>T, XR_951556.2:n.175G>A, XR_951556.1:n.479G>T, XR_951556.1:n.479G>A, XR_951554.3:n.163G>T, XR_951554.3:n.163G>A, XR_951554.2:n.175G>T, XR_951554.2:n.175G>A, XR_951554.1:n.479G>T, XR_951554.1:n.479G>A, XR_951557.3:n.163G>T, XR_951557.3:n.163G>A, XR_951557.2:n.175G>T, XR_951557.2:n.175G>A, XR_951557.1:n.479G>T, XR_951557.1:n.479G>A, XM_011546387.3:c.-43G>T, XM_011546387.3:c.-43G>A, XM_011546387.2:c.-43G>T, XM_011546387.2:c.-43G>A, XM_011546387.1:c.-43G>T, XM_011546387.1:c.-43G>A, XR_951555.3:n.163G>T, XR_951555.3:n.163G>A, XR_951555.2:n.175G>T, XR_951555.2:n.175G>A, XR_951555.1:n.479G>T, XR_951555.1:n.479G>A, XM_011546391.3:c.-43G>T, XM_011546391.3:c.-43G>A, XM_011546391.2:c.-43G>T, XM_011546391.2:c.-43G>A, XM_011546391.1:c.-43G>T, XM_011546391.1:c.-43G>A, NM_001363805.1:c.-43G>T, NM_001363805.1:c.-43G>A, NM_001352769.1:c.-43G>T, NM_001352769.1:c.-43G>A, NM_001103154.2:c.-43G>T, NM_001103154.2:c.-43G>A, NM_001103154.1:c.-43G>T, NM_001103154.1:c.-43G>A, XM_017030176.2:c.-43G>T, XM_017030176.2:c.-43G>A, XM_017030176.1:c.-43G>T, XM_017030176.1:c.-43G>A, XM_024452507.2:c.-43G>T, XM_024452507.2:c.-43G>A, XM_024452507.1:c.-43G>T, XM_024452507.1:c.-43G>A, XM_024452506.2:c.-43G>T, XM_024452506.2:c.-43G>A, XM_024452506.1:c.-43G>T, XM_024452506.1:c.-43G>A, NM_001330240.1:c.-43G>T, NM_001330240.1:c.-43G>A, XR_007068576.1:n.160G>T, XR_007068576.1:n.160G>A, XM_047442815.1:c.-43G>T, XM_047442815.1:c.-43G>A, XM_047442814.1:c.-43G>T, XM_047442814.1:c.-43G>A

Select item 14706550899.

rs1470655089 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 17:46274699 (GRCh38)
17:44352065 (GRCh37)
Canonical SPDI:: NC_000017.11:46274698:C:A
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.46274699C>A, NC_000017.10:g.44352065C>A, NT_167251.2:g.511912G>T, NT_167251.1:g.513905G>T, NT_187663.1:g.977088C>A, NM_001103154.2:c.*741G>T

Select item 147006179210.

rs1470061792 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:46274294 (GRCh38)
17:44351660 (GRCh37)
Canonical SPDI:: NC_000017.11:46274293:T:C
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_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_000017.11:g.46274294T>C, NC_000017.10:g.44351660T>C, NT_167251.2:g.512317A>G, NT_167251.1:g.514310A>G, NT_187663.1:g.976683T>C, NM_001103154.2:c.*1146A>G

Select item 146999629611.

rs1469996296 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:46275073 (GRCh38)
17:44352439 (GRCh37)
Canonical SPDI:: NC_000017.11:46275072:G:T
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.46275073G>T, NC_000017.10:g.44352439G>T, NT_167251.2:g.511541C>A, NT_167251.1:g.513534C>A, NT_187663.1:g.977462G>T, NM_001103154.2:c.*367C>A

Select item 146948651412.

rs1469486514 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:46274701 (GRCh38)
17:44352067 (GRCh37)
Canonical SPDI:: NC_000017.11:46274700:G:T
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
HGVS:: NC_000017.11:g.46274701G>T, NC_000017.10:g.44352067G>T, NT_167251.2:g.511910C>A, NT_167251.1:g.513903C>A, NT_187663.1:g.977090G>T, NM_001103154.2:c.*739C>A

Select item 146619372313.

rs1466193723 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:46352900 (GRCh38)
17:44430266 (GRCh37)
Canonical SPDI:: NC_000017.11:46352899:T:C
Gene:: ARL17B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000017.11:g.46352900T>C, NC_000017.10:g.44430266T>C, NT_167251.2:g.398437A>G, NT_167251.1:g.400430A>G, NM_001039083.5:c.179A>G, NM_001039083.4:c.179A>G, NM_001039083.3:c.179A>G, XR_951553.4:n.384A>G, XR_951553.3:n.402A>G, XR_951553.2:n.396A>G, XR_951553.1:n.700A>G, XM_006725284.4:c.179A>G, XM_006725284.3:c.179A>G, XM_006725284.2:c.179A>G, XM_006725284.1:c.179A>G, XM_011546390.4:c.179A>G, XM_011546390.3:c.179A>G, XM_011546390.2:c.179A>G, XM_011546390.1:c.179A>G, XM_006725288.4:c.179A>G, XM_006725288.3:c.179A>G, XM_006725288.2:c.179A>G, XM_006725288.1:c.179A>G, XM_011546389.3:c.179A>G, XM_011546389.2:c.179A>G, XM_011546389.1:c.179A>G, XR_951556.3:n.384A>G, XR_951556.2:n.396A>G, XR_951556.1:n.700A>G, XR_951554.3:n.384A>G, XR_951554.2:n.396A>G, XR_951554.1:n.700A>G, XR_951557.3:n.384A>G, XR_951557.2:n.396A>G, XR_951557.1:n.700A>G, XM_011546387.3:c.179A>G, XM_011546387.2:c.179A>G, XM_011546387.1:c.179A>G, XR_951555.3:n.384A>G, XR_951555.2:n.396A>G, XR_951555.1:n.700A>G, XM_011546391.3:c.179A>G, XM_011546391.2:c.179A>G, XM_011546391.1:c.179A>G, NM_001352769.1:c.179A>G, NM_001103154.2:c.179A>G, NM_001103154.1:c.179A>G, XM_017030176.2:c.179A>G, XM_017030176.1:c.179A>G, XM_024452506.2:c.179A>G, XM_024452506.1:c.179A>G, NM_001363805.1:c.179A>G, NM_001330240.1:c.179A>G, XM_024452507.2:c.179A>G, XM_024452507.1:c.179A>G, XR_007068576.1:n.381A>G, XM_047442814.1:c.179A>G, XM_047442815.1:c.179A>G, NP_001034172.3:p.Asn60Ser, NP_001339698.1:p.Asn60Ser, NP_001096624.1:p.Asn60Ser, NP_001350734.1:p.Asn60Ser, NP_001317169.1:p.Asn60Ser

Select item 146531527614.

rs1465315276 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:46275239 (GRCh38)
17:44352605 (GRCh37)
Canonical SPDI:: NC_000017.11:46275238:T:C
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.00005/7 (GnomAD)
HGVS:: NC_000017.11:g.46275239T>C, NC_000017.10:g.44352605T>C, NT_167251.2:g.511375A>G, NT_167251.1:g.513368A>G, NT_187663.1:g.977628T>C, NM_001103154.2:c.*201A>G

Select item 146424985115.

rs1464249851 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:46274582 (GRCh38)
17:44351948 (GRCh37)
Canonical SPDI:: NC_000017.11:46274581:C:T
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000342/1 (KOREAN)
HGVS:: NC_000017.11:g.46274582C>T, NC_000017.10:g.44351948C>T, NT_167251.2:g.512029G>A, NT_167251.1:g.514022G>A, NT_187663.1:g.976971C>T, NM_001103154.2:c.*858G>A

Select item 146144478516.

rs1461444785 [Homo sapiens]

Variant type:: SNV:
Alleles:: GAAACGGAG>-
Chromosome:: no mapping
Canonical SPDI:

Select item 145764593517.

rs1457645935 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:46274666 (GRCh38)
17:44352032 (GRCh37)
Canonical SPDI:: NC_000017.11:46274665:A:G
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000043/6 (GnomAD)
G=0.000045/12 (TOPMED)
HGVS:: NC_000017.11:g.46274666A>G, NC_000017.10:g.44352032A>G, NT_167251.2:g.511945T>C, NT_167251.1:g.513938T>C, NT_187663.1:g.977055A>G, NM_001103154.2:c.*774T>C

Select item 145746928518.

rs1457469285 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:46274993 (GRCh38)
17:44352359 (GRCh37)
Canonical SPDI:: NC_000017.11:46274992:A:C
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000017.11:g.46274993A>C, NC_000017.10:g.44352359A>C, NT_167251.2:g.511620T>G, NT_167251.1:g.513613T>G, NT_187663.1:g.977382A>C, NM_001103154.2:c.*447T>G

Select item 145707741319.

rs1457077413 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:46361767 (GRCh38)
17:44439133 (GRCh37)
Canonical SPDI:: NC_000017.11:46361766:G:A
Gene:: ARL17B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00059/7 (ALFA)
A=0.000738/90 (GnomAD)
A=0.000929/246 (TOPMED)
A=0.001093/7 (1000Genomes)
HGVS:: NC_000017.11:g.46361767G>A, NC_000017.10:g.44439133G>A, NG_056914.1:g.165G>A, NT_167251.2:g.389620C>T, NT_167251.1:g.391613C>T, XR_951553.4:n.97C>T, XR_951553.3:n.115C>T, XR_951553.2:n.109C>T, XR_951553.1:n.413C>T, XM_006725284.4:c.-109C>T, XM_006725284.3:c.-109C>T, XM_006725284.2:c.-109C>T, XM_011546390.4:c.-109C>T, XM_011546390.3:c.-109C>T, XM_011546390.2:c.-109C>T, XM_011546390.1:c.-109C>T, XM_006725288.4:c.-109C>T, XM_006725288.3:c.-109C>T, XM_006725288.2:c.-109C>T, XM_006725288.1:c.-109C>T, XM_011546389.3:c.-109C>T, XM_011546389.2:c.-109C>T, XM_011546389.1:c.-109C>T, XR_951556.3:n.97C>T, XR_951556.2:n.109C>T, XR_951556.1:n.413C>T, XR_951554.3:n.97C>T, XR_951554.2:n.109C>T, XR_951554.1:n.413C>T, XR_951557.3:n.97C>T, XR_951557.2:n.109C>T, XR_951557.1:n.413C>T, XM_011546387.3:c.-109C>T, XM_011546387.2:c.-109C>T, XM_011546387.1:c.-109C>T, XR_951555.3:n.97C>T, XR_951555.2:n.109C>T, XR_951555.1:n.413C>T, XM_011546391.3:c.-109C>T, XM_011546391.2:c.-109C>T, XM_011546391.1:c.-109C>T, NM_001103154.2:c.-109C>T, NM_001103154.1:c.-109C>T, XM_017030176.2:c.-109C>T, XM_017030176.1:c.-109C>T, XM_024452507.2:c.-109C>T, XM_024452507.1:c.-109C>T, XM_024452506.2:c.-109C>T, XM_024452506.1:c.-109C>T, NM_001352769.1:c.-109C>T, NM_001363805.1:c.-109C>T, NM_001330240.1:c.-109C>T, XR_007068576.1:n.94C>T, XM_047442814.1:c.-109C>T, XM_047442815.1:c.-109C>T

Select item 145589250320.

rs1455892503 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:46274890 (GRCh38)
17:44352256 (GRCh37)
Canonical SPDI:: NC_000017.11:46274889:T:C
Gene:: LRRC37A (Varview), ARL17B (Varview), LOC124904014 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,3_prime_UTR_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_000017.11:g.46274890T>C, NC_000017.10:g.44352256T>C, NT_167251.2:g.511723A>G, NT_167251.1:g.513716A>G, NT_187663.1:g.977279T>C, NM_001103154.2:c.*550A>G

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