SNP Links for Nucleotide (Select 1284806338) - SNP

Select item 14359947481.

rs1435994748 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 5:135941776 (GRCh38)
5:135277465 (GRCh37)
Canonical SPDI:: NC_000005.10:135941775:A:T
Gene:: FBXL21P (Varview)
Functional Consequence:: 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)
HGVS:: NC_000005.10:g.135941776A>T, NC_000005.9:g.135277465A>T, NR_152421.1:n.2181A>T, NR_152420.1:n.2177A>T

Select item 13706335692.

rs1370633569 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:135940991 (GRCh38)
5:135276680 (GRCh37)
Canonical SPDI:: NC_000005.10:135940990:T:C
Gene:: FBXL21P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.135940991T>C, NC_000005.9:g.135276680T>C, NR_152421.1:n.1396T>C, NR_152420.1:n.1392T>C

Select item 13358114083.

rs1335811408 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 5:135930308 (GRCh38)
5:135265997 (GRCh37)
Canonical SPDI:: NC_000005.10:135930307:G:A,NC_000005.10:135930307:G:T
Gene:: FBXL21P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000005.10:g.135930308G>A, NC_000005.10:g.135930308G>T, NC_000005.9:g.135265997G>A, NC_000005.9:g.135265997G>T, NR_152421.1:n.12G>A, NR_152421.1:n.12G>T, NR_152420.1:n.12G>A, NR_152420.1:n.12G>T

Select item 13266142904.

rs1326614290 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:135936849 (GRCh38)
5:135272538 (GRCh37)
Canonical SPDI:: NC_000005.10:135936848:T:C
Gene:: FBXL21P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000005.10:g.135936849T>C, NC_000005.9:g.135272538T>C, NM_012159.4:c.255T>C, NR_152421.1:n.659T>C, NR_152420.1:n.655T>C, NR_132347.1:n.737T>C

Select item 12958179405.

rs1295817940 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 5:135941933 (GRCh38)
5:135277622 (GRCh37)
Canonical SPDI:: NC_000005.10:135941932:T:C,NC_000005.10:135941932:T:G
Gene:: FBXL21P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.00031/2 (1000Genomes)
C=0.00034/1 (KOREAN)
HGVS:: NC_000005.10:g.135941933T>C, NC_000005.10:g.135941933T>G, NC_000005.9:g.135277622T>C, NC_000005.9:g.135277622T>G, NR_152421.1:n.2338T>C, NR_152421.1:n.2338T>G, NR_152420.1:n.2334T>C, NR_152420.1:n.2334T>G

Select item 11960735656.

rs1196073565 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 5:135930434 (GRCh38)
5:135266123 (GRCh37)
Canonical SPDI:: NC_000005.10:135930433:C:G
Gene:: FBXL21P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.135930434C>G, NC_000005.9:g.135266123C>G, NM_012159.4:c.-365C>G, NR_152421.1:n.138C>G, NR_152420.1:n.138C>G, NR_132347.1:n.118C>G

Select item 11853905197.

rs1185390519 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 5:135940668 (GRCh38)
5:135276357 (GRCh37)
Canonical SPDI:: NC_000005.10:135940667:A:G,NC_000005.10:135940667:A:T
Gene:: FBXL21P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000051/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.135940668A>G, NC_000005.10:g.135940668A>T, NC_000005.9:g.135276357A>G, NC_000005.9:g.135276357A>T, NR_152421.1:n.1073A>G, NR_152421.1:n.1073A>T, NR_152420.1:n.1069A>G, NR_152420.1:n.1069A>T

Select item 11775557618.

rs1177555761 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTG>- [Show Flanks]
Chromosome:: 5:135941799 (GRCh38)
5:135277488 (GRCh37)
Canonical SPDI:: NC_000005.10:135941795:TTGTTTG:TTG
Gene:: FBXL21P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTG=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000005.10:g.135941799_135941802del, NC_000005.9:g.135277488_135277491del, NR_152421.1:n.2204_2207del, NR_152420.1:n.2200_2203del

dbSNP