SNP Links for Nucleotide (Select 228008292) - SNP

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Select item 14906648021.

rs1490664802 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:85610865 (GRCh38)
6:86320583 (GRCh37)
Canonical SPDI:: NC_000006.12:85610864:T:C
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.85610865T>C, NC_000006.11:g.86320583T>C, NG_031848.1:g.37461A>G, NM_001159677.2:c.*2017A>G, NM_001159677.1:c.*2017A>G, NM_001159674.2:c.*2017A>G, NM_001159674.1:c.*2017A>G, NM_001159673.2:c.*2017A>G, NM_001159673.1:c.*2017A>G, NM_001253771.2:c.*2017A>G, NM_001253771.1:c.*2017A>G, NM_001159676.1:c.*2017A>G, XM_005248635.5:c.*2017A>G, XM_005248635.4:c.*2017A>G, XM_005248635.3:c.*2017A>G, XM_005248635.2:c.*2017A>G, XM_005248635.1:c.*2017A>G, XM_017010178.3:c.*2017A>G, XM_017010178.2:c.*2017A>G, XM_017010178.1:c.*2017A>G, XM_017010176.2:c.*2030A>G, XM_017010176.1:c.*2030A>G, XM_017010177.2:c.*2030A>G, XM_017010177.1:c.*2030A>G, XM_017010179.2:c.*2017A>G, XM_017010179.1:c.*2017A>G, XM_047418081.1:c.*2030A>G, XM_047418082.1:c.*2030A>G, XM_047418083.1:c.*2030A>G

Select item 14889982052.

rs1488998205 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 6:85608373 (GRCh38)
6:86318092 (GRCh37)
Canonical SPDI:: NC_000006.12:85608373:A:AA
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000006.12:g.85608374dup, NC_000006.11:g.86318092dup, NG_031848.1:g.39952dup, NM_001159677.2:c.*4508dup, NM_001159677.1:c.*4508dup, NM_001159674.2:c.*4508dup, NM_001159674.1:c.*4508dup, NM_001159673.2:c.*4508dup, NM_001159673.1:c.*4508dup, NM_001253771.2:c.*4508dup, NM_001253771.1:c.*4508dup, NM_001159676.1:c.*4508dup, XM_005248635.5:c.*4508dup, XM_005248635.4:c.*4508dup, XM_005248635.3:c.*4508dup, XM_005248635.2:c.*4508dup, XM_005248635.1:c.*4508dup, XM_017010178.3:c.*4508dup, XM_017010178.2:c.*4508dup, XM_017010178.1:c.*4508dup, XM_017010176.2:c.*4521dup, XM_017010176.1:c.*4521dup, XM_017010177.2:c.*4521dup, XM_017010177.1:c.*4521dup, XM_017010179.2:c.*4508dup, XM_017010179.1:c.*4508dup, XM_047418081.1:c.*4521dup, XM_047418082.1:c.*4521dup, XM_047418083.1:c.*4521dup

Select item 14889598893.

rs1488959889 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:85607901 (GRCh38)
6:86317619 (GRCh37)
Canonical SPDI:: NC_000006.12:85607900:T:C
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.85607901T>C, NC_000006.11:g.86317619T>C, NG_031848.1:g.40425A>G, NM_001159677.2:c.*4981A>G, NM_001159677.1:c.*4981A>G, NM_001159674.2:c.*4981A>G, NM_001159674.1:c.*4981A>G, NM_001159673.2:c.*4981A>G, NM_001159673.1:c.*4981A>G, NM_001253771.2:c.*4981A>G, NM_001253771.1:c.*4981A>G, NM_001159676.1:c.*4981A>G, XM_005248635.5:c.*4981A>G, XM_017010178.3:c.*4981A>G, XM_017010176.2:c.*4994A>G, XM_017010177.2:c.*4994A>G, XM_017010179.2:c.*4981A>G, XM_047418081.1:c.*4994A>G, XM_047418082.1:c.*4994A>G, XM_047418083.1:c.*4994A>G

Select item 14884933214.

rs1488493321 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:85640555 (GRCh38)
6:86350273 (GRCh37)
Canonical SPDI:: NC_000006.12:85640554:G:A
Gene:: SYNCRIP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant
HGVS:: NC_000006.12:g.85640555G>A, NC_000006.11:g.86350273G>A, NG_031848.1:g.7771C>T, NM_006372.5:c.158C>T, NM_006372.4:c.158C>T, NM_001159677.2:c.158C>T, NM_001159677.1:c.158C>T, NM_001159674.2:c.158C>T, NM_001159674.1:c.158C>T, NM_001159673.2:c.-137C>T, NM_001159673.1:c.-137C>T, NM_001253771.2:c.-273C>T, NM_001253771.1:c.-273C>T, NM_001159676.1:c.158C>T, NM_001159675.1:c.158C>T, XM_005248635.5:c.158C>T, XM_005248635.4:c.158C>T, XM_005248635.3:c.158C>T, XM_005248635.2:c.158C>T, XM_005248635.1:c.158C>T, XM_005248636.4:c.-137C>T, XM_017010178.3:c.158C>T, XM_017010178.2:c.158C>T, XM_017010178.1:c.158C>T, XM_005248637.3:c.158C>T, XM_005248637.2:c.158C>T, XM_005248637.1:c.158C>T, XM_017010176.2:c.158C>T, XM_017010176.1:c.158C>T, XM_017010177.2:c.158C>T, XM_017010177.1:c.158C>T, XM_017010179.2:c.158C>T, XM_017010179.1:c.158C>T, XM_047418081.1:c.158C>T, XM_047418082.1:c.158C>T, XM_047418083.1:c.-137C>T, NM_001410938.1:c.-137C>T, NP_006363.4:p.Ala53Val, NP_001153149.1:p.Ala53Val, NP_001153146.1:p.Ala53Val, NP_001153148.1:p.Ala53Val, NP_001153147.1:p.Ala53Val, XP_005248692.1:p.Ala53Val, XP_016865667.1:p.Ala53Val, XP_005248694.1:p.Ala53Val, XP_016865665.1:p.Ala53Val, XP_016865666.1:p.Ala53Val, XP_016865668.1:p.Ala53Val, XP_047274037.1:p.Ala53Val, XP_047274038.1:p.Ala53Val

Select item 14882559135.

rs1488255913 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:85609641 (GRCh38)
6:86319359 (GRCh37)
Canonical SPDI:: NC_000006.12:85609640:T:C
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.85609641T>C, NC_000006.11:g.86319359T>C, NG_031848.1:g.38685A>G, NM_001159677.2:c.*3241A>G, NM_001159677.1:c.*3241A>G, NM_001159674.2:c.*3241A>G, NM_001159674.1:c.*3241A>G, NM_001159673.2:c.*3241A>G, NM_001159673.1:c.*3241A>G, NM_001253771.2:c.*3241A>G, NM_001253771.1:c.*3241A>G, NM_001159676.1:c.*3241A>G, XM_005248635.5:c.*3241A>G, XM_005248635.4:c.*3241A>G, XM_005248635.3:c.*3241A>G, XM_005248635.2:c.*3241A>G, XM_005248635.1:c.*3241A>G, XM_017010178.3:c.*3241A>G, XM_017010178.2:c.*3241A>G, XM_017010178.1:c.*3241A>G, XM_017010176.2:c.*3254A>G, XM_017010176.1:c.*3254A>G, XM_017010177.2:c.*3254A>G, XM_017010177.1:c.*3254A>G, XM_017010179.2:c.*3241A>G, XM_017010179.1:c.*3241A>G, XM_047418081.1:c.*3254A>G, XM_047418082.1:c.*3254A>G, XM_047418083.1:c.*3254A>G

Select item 14868432356.

rs1486843235 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:85611063 (GRCh38)
6:86320781 (GRCh37)
Canonical SPDI:: NC_000006.12:85611062:T:C
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.85611063T>C, NC_000006.11:g.86320781T>C, NG_031848.1:g.37263A>G, NM_001159677.2:c.*1819A>G, NM_001159677.1:c.*1819A>G, NM_001159674.2:c.*1819A>G, NM_001159674.1:c.*1819A>G, NM_001159673.2:c.*1819A>G, NM_001159673.1:c.*1819A>G, NM_001253771.2:c.*1819A>G, NM_001253771.1:c.*1819A>G, NM_001159676.1:c.*1819A>G, XM_005248635.5:c.*1819A>G, XM_005248635.4:c.*1819A>G, XM_005248635.3:c.*1819A>G, XM_005248635.2:c.*1819A>G, XM_005248635.1:c.*1819A>G, XM_017010178.3:c.*1819A>G, XM_017010178.2:c.*1819A>G, XM_017010178.1:c.*1819A>G, XM_017010176.2:c.*1832A>G, XM_017010176.1:c.*1832A>G, XM_017010177.2:c.*1832A>G, XM_017010177.1:c.*1832A>G, XM_017010179.2:c.*1819A>G, XM_017010179.1:c.*1819A>G, XM_047418081.1:c.*1832A>G, XM_047418082.1:c.*1832A>G, XM_047418083.1:c.*1832A>G

Select item 14857269017.

rs1485726901 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:85610577 (GRCh38)
6:86320295 (GRCh37)
Canonical SPDI:: NC_000006.12:85610576:C:T
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_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_000006.12:g.85610577C>T, NC_000006.11:g.86320295C>T, NG_031848.1:g.37749G>A, NM_001159677.2:c.*2305G>A, NM_001159677.1:c.*2305G>A, NM_001159674.2:c.*2305G>A, NM_001159674.1:c.*2305G>A, NM_001159673.2:c.*2305G>A, NM_001159673.1:c.*2305G>A, NM_001253771.2:c.*2305G>A, NM_001253771.1:c.*2305G>A, NM_001159676.1:c.*2305G>A, XM_005248635.5:c.*2305G>A, XM_005248635.4:c.*2305G>A, XM_005248635.3:c.*2305G>A, XM_005248635.2:c.*2305G>A, XM_005248635.1:c.*2305G>A, XM_017010178.3:c.*2305G>A, XM_017010178.2:c.*2305G>A, XM_017010178.1:c.*2305G>A, XM_017010176.2:c.*2318G>A, XM_017010176.1:c.*2318G>A, XM_017010177.2:c.*2318G>A, XM_017010177.1:c.*2318G>A, XM_017010179.2:c.*2305G>A, XM_017010179.1:c.*2305G>A, XM_047418081.1:c.*2318G>A, XM_047418082.1:c.*2318G>A, XM_047418083.1:c.*2318G>A

Select item 14849902938.

rs1484990293 [Homo sapiens]

Variant type:: DEL
Alleles:: CTTT>- [Show Flanks]
Chromosome:: 6:85610581 (GRCh38)
6:86320299 (GRCh37)
Canonical SPDI:: NC_000006.12:85610580:CTTT:
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.85610581_85610584del, NC_000006.11:g.86320299_86320302del, NG_031848.1:g.37742_37745del, NM_001159677.2:c.*2298_*2301del, NM_001159677.1:c.*2298_*2301del, NM_001159674.2:c.*2298_*2301del, NM_001159674.1:c.*2298_*2301del, NM_001159673.2:c.*2298_*2301del, NM_001159673.1:c.*2298_*2301del, NM_001253771.2:c.*2298_*2301del, NM_001253771.1:c.*2298_*2301del, NM_001159676.1:c.*2298_*2301del, XM_005248635.5:c.*2298_*2301del, XM_005248635.4:c.*2298_*2301del, XM_005248635.3:c.*2298_*2301del, XM_005248635.2:c.*2298_*2301del, XM_005248635.1:c.*2298_*2301del, XM_017010178.3:c.*2298_*2301del, XM_017010178.2:c.*2298_*2301del, XM_017010178.1:c.*2298_*2301del, XM_017010176.2:c.*2311_*2314del, XM_017010176.1:c.*2311_*2314del, XM_017010177.2:c.*2311_*2314del, XM_017010177.1:c.*2311_*2314del, XM_017010179.2:c.*2298_*2301del, XM_017010179.1:c.*2298_*2301del, XM_047418081.1:c.*2311_*2314del, XM_047418082.1:c.*2311_*2314del, XM_047418083.1:c.*2311_*2314del

Select item 14848806349.

rs1484880634 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 6:85607796 (GRCh38)
6:86317514 (GRCh37)
Canonical SPDI:: NC_000006.12:85607795:T:C,NC_000006.12:85607795:T:G
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000006.12:g.85607796T>C, NC_000006.12:g.85607796T>G, NC_000006.11:g.86317514T>C, NC_000006.11:g.86317514T>G, NG_031848.1:g.40530A>G, NG_031848.1:g.40530A>C, NM_001159677.2:c.*5086A>G, NM_001159677.2:c.*5086A>C, NM_001159677.1:c.*5086A>G, NM_001159677.1:c.*5086A>C, NM_001159674.2:c.*5086A>G, NM_001159674.2:c.*5086A>C, NM_001159674.1:c.*5086A>G, NM_001159674.1:c.*5086A>C, NM_001159673.2:c.*5086A>G, NM_001159673.2:c.*5086A>C, NM_001159673.1:c.*5086A>G, NM_001159673.1:c.*5086A>C, NM_001253771.2:c.*5086A>G, NM_001253771.2:c.*5086A>C, NM_001253771.1:c.*5086A>G, NM_001253771.1:c.*5086A>C, NM_001159676.1:c.*5086A>G, NM_001159676.1:c.*5086A>C, XM_005248635.5:c.*5086A>G, XM_005248635.5:c.*5086A>C, XM_017010178.3:c.*5086A>G, XM_017010178.3:c.*5086A>C, XM_017010176.2:c.*5099A>G, XM_017010176.2:c.*5099A>C, XM_017010177.2:c.*5099A>G, XM_017010177.2:c.*5099A>C, XM_017010179.2:c.*5086A>G, XM_017010179.2:c.*5086A>C, XM_047418081.1:c.*5099A>G, XM_047418081.1:c.*5099A>C, XM_047418082.1:c.*5099A>G, XM_047418082.1:c.*5099A>C, XM_047418083.1:c.*5099A>G, XM_047418083.1:c.*5099A>C

Select item 148431243210.

rs1484312432 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:85607853 (GRCh38)
6:86317571 (GRCh37)
Canonical SPDI:: NC_000006.12:85607852:G:A
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.85607853G>A, NC_000006.11:g.86317571G>A, NG_031848.1:g.40473C>T, NM_001159677.2:c.*5029C>T, NM_001159677.1:c.*5029C>T, NM_001159674.2:c.*5029C>T, NM_001159674.1:c.*5029C>T, NM_001159673.2:c.*5029C>T, NM_001159673.1:c.*5029C>T, NM_001253771.2:c.*5029C>T, NM_001253771.1:c.*5029C>T, NM_001159676.1:c.*5029C>T, XM_005248635.5:c.*5029C>T, XM_017010178.3:c.*5029C>T, XM_017010176.2:c.*5042C>T, XM_017010177.2:c.*5042C>T, XM_017010179.2:c.*5029C>T, XM_047418081.1:c.*5042C>T, XM_047418082.1:c.*5042C>T, XM_047418083.1:c.*5042C>T

Select item 148404213811.

rs1484042138 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 6:85609004 (GRCh38)
6:86318722 (GRCh37)
Canonical SPDI:: NC_000006.12:85609003:CT:
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.85609004_85609005del, NC_000006.11:g.86318722_86318723del, NG_031848.1:g.39321_39322del, NM_001159677.2:c.*3877_*3878del, NM_001159677.1:c.*3877_*3878del, NM_001159674.2:c.*3877_*3878del, NM_001159674.1:c.*3877_*3878del, NM_001159673.2:c.*3877_*3878del, NM_001159673.1:c.*3877_*3878del, NM_001253771.2:c.*3877_*3878del, NM_001253771.1:c.*3877_*3878del, NM_001159676.1:c.*3877_*3878del, XM_005248635.5:c.*3877_*3878del, XM_005248635.4:c.*3877_*3878del, XM_005248635.3:c.*3877_*3878del, XM_005248635.2:c.*3877_*3878del, XM_005248635.1:c.*3877_*3878del, XM_017010178.3:c.*3877_*3878del, XM_017010178.2:c.*3877_*3878del, XM_017010178.1:c.*3877_*3878del, XM_017010176.2:c.*3890_*3891del, XM_017010176.1:c.*3890_*3891del, XM_017010177.2:c.*3890_*3891del, XM_017010177.1:c.*3890_*3891del, XM_017010179.2:c.*3877_*3878del, XM_017010179.1:c.*3877_*3878del, XM_047418081.1:c.*3890_*3891del, XM_047418082.1:c.*3890_*3891del, XM_047418083.1:c.*3890_*3891del

Select item 148357172912.

rs1483571729 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:85611882 (GRCh38)
6:86321600 (GRCh37)
Canonical SPDI:: NC_000006.12:85611881:A:G
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.85611882A>G, NC_000006.11:g.86321600A>G, NG_031848.1:g.36444T>C, NM_001159677.2:c.*1000T>C, NM_001159677.1:c.*1000T>C, NM_001159674.2:c.*1000T>C, NM_001159674.1:c.*1000T>C, NM_001159673.2:c.*1000T>C, NM_001159673.1:c.*1000T>C, NM_001253771.2:c.*1000T>C, NM_001253771.1:c.*1000T>C, NM_001159676.1:c.*1000T>C, XM_005248635.5:c.*1000T>C, XM_005248635.4:c.*1000T>C, XM_005248635.3:c.*1000T>C, XM_005248635.2:c.*1000T>C, XM_005248635.1:c.*1000T>C, XM_017010178.3:c.*1000T>C, XM_017010178.2:c.*1000T>C, XM_017010178.1:c.*1000T>C, XM_017010176.2:c.*1013T>C, XM_017010176.1:c.*1013T>C, XM_017010177.2:c.*1013T>C, XM_017010177.1:c.*1013T>C, XM_017010179.2:c.*1000T>C, XM_017010179.1:c.*1000T>C, XM_047418081.1:c.*1013T>C, XM_047418082.1:c.*1013T>C, XM_047418083.1:c.*1013T>C

Select item 148338908913.

rs1483389089 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:85609002 (GRCh38)
6:86318720 (GRCh37)
Canonical SPDI:: NC_000006.12:85609001:C:A
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.85609002C>A, NC_000006.11:g.86318720C>A, NG_031848.1:g.39324G>T, NM_001159677.2:c.*3880G>T, NM_001159677.1:c.*3880G>T, NM_001159674.2:c.*3880G>T, NM_001159674.1:c.*3880G>T, NM_001159673.2:c.*3880G>T, NM_001159673.1:c.*3880G>T, NM_001253771.2:c.*3880G>T, NM_001253771.1:c.*3880G>T, NM_001159676.1:c.*3880G>T, XM_005248635.5:c.*3880G>T, XM_005248635.4:c.*3880G>T, XM_005248635.3:c.*3880G>T, XM_005248635.2:c.*3880G>T, XM_005248635.1:c.*3880G>T, XM_017010178.3:c.*3880G>T, XM_017010178.2:c.*3880G>T, XM_017010178.1:c.*3880G>T, XM_017010176.2:c.*3893G>T, XM_017010176.1:c.*3893G>T, XM_017010177.2:c.*3893G>T, XM_017010177.1:c.*3893G>T, XM_017010179.2:c.*3880G>T, XM_017010179.1:c.*3880G>T, XM_047418081.1:c.*3893G>T, XM_047418082.1:c.*3893G>T, XM_047418083.1:c.*3893G>T

Select item 148331805714.

rs1483318057 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:85609375 (GRCh38)
6:86319093 (GRCh37)
Canonical SPDI:: NC_000006.12:85609374:G:A
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.85609375G>A, NC_000006.11:g.86319093G>A, NG_031848.1:g.38951C>T, NM_001159677.2:c.*3507C>T, NM_001159677.1:c.*3507C>T, NM_001159674.2:c.*3507C>T, NM_001159674.1:c.*3507C>T, NM_001159673.2:c.*3507C>T, NM_001159673.1:c.*3507C>T, NM_001253771.2:c.*3507C>T, NM_001253771.1:c.*3507C>T, NM_001159676.1:c.*3507C>T, XM_005248635.5:c.*3507C>T, XM_005248635.4:c.*3507C>T, XM_005248635.3:c.*3507C>T, XM_005248635.2:c.*3507C>T, XM_005248635.1:c.*3507C>T, XM_017010178.3:c.*3507C>T, XM_017010178.2:c.*3507C>T, XM_017010178.1:c.*3507C>T, XM_017010176.2:c.*3520C>T, XM_017010176.1:c.*3520C>T, XM_017010177.2:c.*3520C>T, XM_017010177.1:c.*3520C>T, XM_017010179.2:c.*3507C>T, XM_017010179.1:c.*3507C>T, XM_047418081.1:c.*3520C>T, XM_047418082.1:c.*3520C>T, XM_047418083.1:c.*3520C>T

Select item 148266014015.

rs1482660140 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:85610204 (GRCh38)
6:86319922 (GRCh37)
Canonical SPDI:: NC_000006.12:85610203:T:C
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_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.85610204T>C, NC_000006.11:g.86319922T>C, NG_031848.1:g.38122A>G, NM_001159677.2:c.*2678A>G, NM_001159677.1:c.*2678A>G, NM_001159674.2:c.*2678A>G, NM_001159674.1:c.*2678A>G, NM_001159673.2:c.*2678A>G, NM_001159673.1:c.*2678A>G, NM_001253771.2:c.*2678A>G, NM_001253771.1:c.*2678A>G, NM_001159676.1:c.*2678A>G, XM_005248635.5:c.*2678A>G, XM_005248635.4:c.*2678A>G, XM_005248635.3:c.*2678A>G, XM_005248635.2:c.*2678A>G, XM_005248635.1:c.*2678A>G, XM_017010178.3:c.*2678A>G, XM_017010178.2:c.*2678A>G, XM_017010178.1:c.*2678A>G, XM_017010176.2:c.*2691A>G, XM_017010176.1:c.*2691A>G, XM_017010177.2:c.*2691A>G, XM_017010177.1:c.*2691A>G, XM_017010179.2:c.*2678A>G, XM_017010179.1:c.*2678A>G, XM_047418081.1:c.*2691A>G, XM_047418082.1:c.*2691A>G, XM_047418083.1:c.*2691A>G

Select item 148243493816.

rs1482434938 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 6:85609353 (GRCh38)
6:86319071 (GRCh37)
Canonical SPDI:: NC_000006.12:85609352:A:C
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.85609353A>C, NC_000006.11:g.86319071A>C, NG_031848.1:g.38973T>G, NM_001159677.2:c.*3529T>G, NM_001159677.1:c.*3529T>G, NM_001159674.2:c.*3529T>G, NM_001159674.1:c.*3529T>G, NM_001159673.2:c.*3529T>G, NM_001159673.1:c.*3529T>G, NM_001253771.2:c.*3529T>G, NM_001253771.1:c.*3529T>G, NM_001159676.1:c.*3529T>G, XM_005248635.5:c.*3529T>G, XM_005248635.4:c.*3529T>G, XM_005248635.3:c.*3529T>G, XM_005248635.2:c.*3529T>G, XM_005248635.1:c.*3529T>G, XM_017010178.3:c.*3529T>G, XM_017010178.2:c.*3529T>G, XM_017010178.1:c.*3529T>G, XM_017010176.2:c.*3542T>G, XM_017010176.1:c.*3542T>G, XM_017010177.2:c.*3542T>G, XM_017010177.1:c.*3542T>G, XM_017010179.2:c.*3529T>G, XM_017010179.1:c.*3529T>G, XM_047418081.1:c.*3542T>G, XM_047418082.1:c.*3542T>G, XM_047418083.1:c.*3542T>G

Select item 148105023817.

rs1481050238 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:85610780 (GRCh38)
6:86320498 (GRCh37)
Canonical SPDI:: NC_000006.12:85610779:C:T
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.85610780C>T, NC_000006.11:g.86320498C>T, NG_031848.1:g.37546G>A, NM_001159677.2:c.*2102G>A, NM_001159677.1:c.*2102G>A, NM_001159674.2:c.*2102G>A, NM_001159674.1:c.*2102G>A, NM_001159673.2:c.*2102G>A, NM_001159673.1:c.*2102G>A, NM_001253771.2:c.*2102G>A, NM_001253771.1:c.*2102G>A, NM_001159676.1:c.*2102G>A, XM_005248635.5:c.*2102G>A, XM_005248635.4:c.*2102G>A, XM_005248635.3:c.*2102G>A, XM_005248635.2:c.*2102G>A, XM_005248635.1:c.*2102G>A, XM_017010178.3:c.*2102G>A, XM_017010178.2:c.*2102G>A, XM_017010178.1:c.*2102G>A, XM_017010176.2:c.*2115G>A, XM_017010176.1:c.*2115G>A, XM_017010177.2:c.*2115G>A, XM_017010177.1:c.*2115G>A, XM_017010179.2:c.*2102G>A, XM_017010179.1:c.*2102G>A, XM_047418081.1:c.*2115G>A, XM_047418082.1:c.*2115G>A, XM_047418083.1:c.*2115G>A

Select item 148101495918.

rs1481014959 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTAA>- [Show Flanks]
Chromosome:: 6:85610617 (GRCh38)
6:86320335 (GRCh37)
Canonical SPDI:: NC_000006.12:85610614:AAGTAA:AA
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0.000054/1 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
-=0.000071/1 (TOMMO)
-=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.85610617_85610620del, NC_000006.11:g.86320335_86320338del, NG_031848.1:g.37708_37711del, NM_001159677.2:c.*2264_*2267del, NM_001159677.1:c.*2264_*2267del, NM_001159674.2:c.*2264_*2267del, NM_001159674.1:c.*2264_*2267del, NM_001159673.2:c.*2264_*2267del, NM_001159673.1:c.*2264_*2267del, NM_001253771.2:c.*2264_*2267del, NM_001253771.1:c.*2264_*2267del, NM_001159676.1:c.*2264_*2267del, XM_005248635.5:c.*2264_*2267del, XM_005248635.4:c.*2264_*2267del, XM_005248635.3:c.*2264_*2267del, XM_005248635.2:c.*2264_*2267del, XM_005248635.1:c.*2264_*2267del, XM_017010178.3:c.*2264_*2267del, XM_017010178.2:c.*2264_*2267del, XM_017010178.1:c.*2264_*2267del, XM_017010176.2:c.*2277_*2280del, XM_017010176.1:c.*2277_*2280del, XM_017010177.2:c.*2277_*2280del, XM_017010177.1:c.*2277_*2280del, XM_017010179.2:c.*2264_*2267del, XM_017010179.1:c.*2264_*2267del, XM_047418081.1:c.*2277_*2280del, XM_047418082.1:c.*2277_*2280del, XM_047418083.1:c.*2277_*2280del

Select item 148082519219.

rs1480825192 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:85609793 (GRCh38)
6:86319511 (GRCh37)
Canonical SPDI:: NC_000006.12:85609792:T:G
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.85609793T>G, NC_000006.11:g.86319511T>G, NG_031848.1:g.38533A>C, NM_001159677.2:c.*3089A>C, NM_001159677.1:c.*3089A>C, NM_001159674.2:c.*3089A>C, NM_001159674.1:c.*3089A>C, NM_001159673.2:c.*3089A>C, NM_001159673.1:c.*3089A>C, NM_001253771.2:c.*3089A>C, NM_001253771.1:c.*3089A>C, NM_001159676.1:c.*3089A>C, XM_005248635.5:c.*3089A>C, XM_005248635.4:c.*3089A>C, XM_005248635.3:c.*3089A>C, XM_005248635.2:c.*3089A>C, XM_005248635.1:c.*3089A>C, XM_017010178.3:c.*3089A>C, XM_017010178.2:c.*3089A>C, XM_017010178.1:c.*3089A>C, XM_017010176.2:c.*3102A>C, XM_017010176.1:c.*3102A>C, XM_017010177.2:c.*3102A>C, XM_017010177.1:c.*3102A>C, XM_017010179.2:c.*3089A>C, XM_017010179.1:c.*3089A>C, XM_047418081.1:c.*3102A>C, XM_047418082.1:c.*3102A>C, XM_047418083.1:c.*3102A>C

Select item 148043344120.

rs1480433441 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:85611671 (GRCh38)
6:86321389 (GRCh37)
Canonical SPDI:: NC_000006.12:85611670:A:G
Gene:: SYNCRIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.85611671A>G, NC_000006.11:g.86321389A>G, NG_031848.1:g.36655T>C, NM_001159677.2:c.*1211T>C, NM_001159677.1:c.*1211T>C, NM_001159674.2:c.*1211T>C, NM_001159674.1:c.*1211T>C, NM_001159673.2:c.*1211T>C, NM_001159673.1:c.*1211T>C, NM_001253771.2:c.*1211T>C, NM_001253771.1:c.*1211T>C, NM_001159676.1:c.*1211T>C, XM_005248635.5:c.*1211T>C, XM_005248635.4:c.*1211T>C, XM_005248635.3:c.*1211T>C, XM_005248635.2:c.*1211T>C, XM_005248635.1:c.*1211T>C, XM_017010178.3:c.*1211T>C, XM_017010178.2:c.*1211T>C, XM_017010178.1:c.*1211T>C, XM_017010176.2:c.*1224T>C, XM_017010176.1:c.*1224T>C, XM_017010177.2:c.*1224T>C, XM_017010177.1:c.*1224T>C, XM_017010179.2:c.*1211T>C, XM_017010179.1:c.*1211T>C, XM_047418081.1:c.*1224T>C, XM_047418082.1:c.*1224T>C, XM_047418083.1:c.*1224T>C

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