SNP Links for Protein (Select 219842296) - SNP

Links from Protein

Items: 1 to 20 of 197

<< First< Prev

Page of 10

Next >Last >>

Select item 14888640541.

rs1488864054 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:27658401 (GRCh38)
11:27679948 (GRCh37)
Canonical SPDI:: NC_000011.10:27658400:C:T
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.27658401C>T, NC_000011.9:g.27679948C>T, NG_011794.1:g.68658G>A, NM_170735.6:c.164G>A, NM_170735.5:c.164G>A, NM_170731.5:c.188G>A, NM_170731.4:c.188G>A, NM_001709.5:c.164G>A, NM_001709.4:c.164G>A, NM_170732.4:c.164G>A, NM_170733.4:c.164G>A, NM_170733.3:c.164G>A, NM_170734.4:c.209G>A, NM_170734.3:c.209G>A, NM_001143816.2:c.164G>A, NM_001143816.1:c.164G>A, NM_001143811.2:c.164G>A, NM_001143811.1:c.164G>A, NM_001143814.2:c.164G>A, NM_001143814.1:c.164G>A, NM_001143810.2:c.410G>A, NM_001143810.1:c.410G>A, NM_001143813.2:c.164G>A, NM_001143813.1:c.164G>A, NM_001143812.2:c.164G>A, NM_001143812.1:c.164G>A, NM_001143809.2:c.251G>A, NM_001143809.1:c.251G>A, NM_001143808.2:c.164G>A, NM_001143808.1:c.164G>A, NM_001143807.2:c.164G>A, NM_001143807.1:c.164G>A, NM_001143806.1:c.164G>A, NM_001143805.1:c.164G>A, NR_002832.2:n.535C>T, NR_033312.1:n.466C>T, NR_033314.1:n.535C>T, NR_033315.1:n.466C>T, NR_033313.1:n.466C>T, NM_001143815.1:c.164G>A, NP_733931.1:p.Gly55Asp, NP_733927.1:p.Gly63Asp, NP_001700.2:p.Gly55Asp, NP_733928.1:p.Gly55Asp, NP_733929.1:p.Gly55Asp, NP_733930.1:p.Gly70Asp, NP_001137288.1:p.Gly55Asp, NP_001137283.1:p.Gly55Asp, NP_001137286.1:p.Gly55Asp, NP_001137282.1:p.Gly137Asp, NP_001137285.1:p.Gly55Asp, NP_001137284.1:p.Gly55Asp, NP_001137281.1:p.Gly84Asp, NP_001137280.1:p.Gly55Asp, NP_001137279.1:p.Gly55Asp, NP_001137278.1:p.Gly55Asp, NP_001137277.1:p.Gly55Asp

Select item 14840572562.

rs1484057256 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:27658151 (GRCh38)
11:27679698 (GRCh37)
Canonical SPDI:: NC_000011.10:27658150:C:T
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.27658151C>T, NC_000011.9:g.27679698C>T, NG_011794.1:g.68908G>A, NM_170735.6:c.414G>A, NM_170735.5:c.414G>A, NM_170731.5:c.438G>A, NM_170731.4:c.438G>A, NM_001709.5:c.414G>A, NM_001709.4:c.414G>A, NM_170732.4:c.414G>A, NM_170733.4:c.414G>A, NM_170733.3:c.414G>A, NM_170734.4:c.459G>A, NM_170734.3:c.459G>A, NM_001143816.2:c.414G>A, NM_001143816.1:c.414G>A, NM_001143811.2:c.414G>A, NM_001143811.1:c.414G>A, NM_001143814.2:c.414G>A, NM_001143814.1:c.414G>A, NM_001143810.2:c.660G>A, NM_001143810.1:c.660G>A, NM_001143813.2:c.414G>A, NM_001143813.1:c.414G>A, NM_001143812.2:c.414G>A, NM_001143812.1:c.414G>A, NM_001143809.2:c.501G>A, NM_001143809.1:c.501G>A, NM_001143808.2:c.414G>A, NM_001143808.1:c.414G>A, NM_001143807.2:c.414G>A, NM_001143807.1:c.414G>A, NM_001143806.1:c.414G>A, NM_001143805.1:c.414G>A, NM_001143815.1:c.414G>A

Select item 14829398983.

rs1482939898 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:27658487 (GRCh38)
11:27680034 (GRCh37)
Canonical SPDI:: NC_000011.10:27658486:G:T
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.27658487G>T, NC_000011.9:g.27680034G>T, NG_011794.1:g.68572C>A, NM_170735.6:c.78C>A, NM_170735.5:c.78C>A, NM_170731.5:c.102C>A, NM_170731.4:c.102C>A, NM_001709.5:c.78C>A, NM_001709.4:c.78C>A, NM_170732.4:c.78C>A, NM_170733.4:c.78C>A, NM_170733.3:c.78C>A, NM_170734.4:c.123C>A, NM_170734.3:c.123C>A, NM_001143816.2:c.78C>A, NM_001143816.1:c.78C>A, NM_001143811.2:c.78C>A, NM_001143811.1:c.78C>A, NM_001143814.2:c.78C>A, NM_001143814.1:c.78C>A, NM_001143810.2:c.324C>A, NM_001143810.1:c.324C>A, NM_001143813.2:c.78C>A, NM_001143813.1:c.78C>A, NM_001143812.2:c.78C>A, NM_001143812.1:c.78C>A, NM_001143809.2:c.165C>A, NM_001143809.1:c.165C>A, NM_001143808.2:c.78C>A, NM_001143808.1:c.78C>A, NM_001143807.2:c.78C>A, NM_001143807.1:c.78C>A, NM_001143806.1:c.78C>A, NM_001143805.1:c.78C>A, NM_001143815.1:c.78C>A

Select item 14768994054.

rs1476899405 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:27658404 (GRCh38)
11:27679951 (GRCh37)
Canonical SPDI:: NC_000011.10:27658403:C:T
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.27658404C>T, NC_000011.9:g.27679951C>T, NG_011794.1:g.68655G>A, NM_170735.6:c.161G>A, NM_170735.5:c.161G>A, NM_170731.5:c.185G>A, NM_170731.4:c.185G>A, NM_001709.5:c.161G>A, NM_001709.4:c.161G>A, NM_170732.4:c.161G>A, NM_170733.4:c.161G>A, NM_170733.3:c.161G>A, NM_170734.4:c.206G>A, NM_170734.3:c.206G>A, NM_001143816.2:c.161G>A, NM_001143816.1:c.161G>A, NM_001143811.2:c.161G>A, NM_001143811.1:c.161G>A, NM_001143814.2:c.161G>A, NM_001143814.1:c.161G>A, NM_001143810.2:c.407G>A, NM_001143810.1:c.407G>A, NM_001143813.2:c.161G>A, NM_001143813.1:c.161G>A, NM_001143812.2:c.161G>A, NM_001143812.1:c.161G>A, NM_001143809.2:c.248G>A, NM_001143809.1:c.248G>A, NM_001143808.2:c.161G>A, NM_001143808.1:c.161G>A, NM_001143807.2:c.161G>A, NM_001143807.1:c.161G>A, NM_001143806.1:c.161G>A, NM_001143805.1:c.161G>A, NR_002832.2:n.538C>T, NR_033312.1:n.469C>T, NR_033314.1:n.538C>T, NR_033315.1:n.469C>T, NR_033313.1:n.469C>T, NM_001143815.1:c.161G>A, NP_733931.1:p.Arg54Lys, NP_733927.1:p.Arg62Lys, NP_001700.2:p.Arg54Lys, NP_733928.1:p.Arg54Lys, NP_733929.1:p.Arg54Lys, NP_733930.1:p.Arg69Lys, NP_001137288.1:p.Arg54Lys, NP_001137283.1:p.Arg54Lys, NP_001137286.1:p.Arg54Lys, NP_001137282.1:p.Arg136Lys, NP_001137285.1:p.Arg54Lys, NP_001137284.1:p.Arg54Lys, NP_001137281.1:p.Arg83Lys, NP_001137280.1:p.Arg54Lys, NP_001137279.1:p.Arg54Lys, NP_001137278.1:p.Arg54Lys, NP_001137277.1:p.Arg54Lys

Select item 14752383845.

rs1475238384 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:27701001 (GRCh38)
11:27722548 (GRCh37)
Canonical SPDI:: NC_000011.10:27701000:G:C
Gene:: BDNF (Varview)
Functional Consequence:: intron_variant,synonymous_variant,genic_upstream_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.27701001G>C, NC_000011.9:g.27722548G>C, NG_011794.1:g.26058C>G, NM_001143811.2:c.-452C>G, NM_001143811.1:c.-452C>G, NM_001143810.2:c.-89C>G, NM_001143810.1:c.-89C>G, NM_001143809.2:c.36C>G, NM_001143809.1:c.36C>G, NM_001143808.2:c.-42C>G, NM_001143808.1:c.-42C>G

Select item 14731802456.

rs1473180245 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:27700996 (GRCh38)
11:27722543 (GRCh37)
Canonical SPDI:: NC_000011.10:27700995:A:G
Gene:: BDNF (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.27700996A>G, NC_000011.9:g.27722543A>G, NG_011794.1:g.26063T>C, NM_001143811.2:c.-447T>C, NM_001143811.1:c.-447T>C, NM_001143810.2:c.-84T>C, NM_001143810.1:c.-84T>C, NM_001143809.2:c.41T>C, NM_001143809.1:c.41T>C, NM_001143808.2:c.-37T>C, NM_001143808.1:c.-37T>C, NP_001137281.1:p.Leu14Pro

Select item 14664117567.

rs1466411756 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:27658496 (GRCh38)
11:27680043 (GRCh37)
Canonical SPDI:: NC_000011.10:27658495:T:G
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.27658496T>G, NC_000011.9:g.27680043T>G, NG_011794.1:g.68563A>C, NM_170735.6:c.69A>C, NM_170735.5:c.69A>C, NM_170731.5:c.93A>C, NM_170731.4:c.93A>C, NM_001709.5:c.69A>C, NM_001709.4:c.69A>C, NM_170732.4:c.69A>C, NM_170733.4:c.69A>C, NM_170733.3:c.69A>C, NM_170734.4:c.114A>C, NM_170734.3:c.114A>C, NM_001143816.2:c.69A>C, NM_001143816.1:c.69A>C, NM_001143811.2:c.69A>C, NM_001143811.1:c.69A>C, NM_001143814.2:c.69A>C, NM_001143814.1:c.69A>C, NM_001143810.2:c.315A>C, NM_001143810.1:c.315A>C, NM_001143813.2:c.69A>C, NM_001143813.1:c.69A>C, NM_001143812.2:c.69A>C, NM_001143812.1:c.69A>C, NM_001143809.2:c.156A>C, NM_001143809.1:c.156A>C, NM_001143808.2:c.69A>C, NM_001143808.1:c.69A>C, NM_001143807.2:c.69A>C, NM_001143807.1:c.69A>C, NM_001143806.1:c.69A>C, NM_001143805.1:c.69A>C, NM_001143815.1:c.69A>C, NP_733931.1:p.Glu23Asp, NP_733927.1:p.Glu31Asp, NP_001700.2:p.Glu23Asp, NP_733928.1:p.Glu23Asp, NP_733929.1:p.Glu23Asp, NP_733930.1:p.Glu38Asp, NP_001137288.1:p.Glu23Asp, NP_001137283.1:p.Glu23Asp, NP_001137286.1:p.Glu23Asp, NP_001137282.1:p.Glu105Asp, NP_001137285.1:p.Glu23Asp, NP_001137284.1:p.Glu23Asp, NP_001137281.1:p.Glu52Asp, NP_001137280.1:p.Glu23Asp, NP_001137279.1:p.Glu23Asp, NP_001137278.1:p.Glu23Asp, NP_001137277.1:p.Glu23Asp

Select item 14646588988.

rs1464658898 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:27658270 (GRCh38)
11:27679817 (GRCh37)
Canonical SPDI:: NC_000011.10:27658269:G:T
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.27658270G>T, NC_000011.9:g.27679817G>T, NG_011794.1:g.68789C>A, NM_170735.6:c.295C>A, NM_170735.5:c.295C>A, NM_170731.5:c.319C>A, NM_170731.4:c.319C>A, NM_001709.5:c.295C>A, NM_001709.4:c.295C>A, NM_170732.4:c.295C>A, NM_170733.4:c.295C>A, NM_170733.3:c.295C>A, NM_170734.4:c.340C>A, NM_170734.3:c.340C>A, NM_001143816.2:c.295C>A, NM_001143816.1:c.295C>A, NM_001143811.2:c.295C>A, NM_001143811.1:c.295C>A, NM_001143814.2:c.295C>A, NM_001143814.1:c.295C>A, NM_001143810.2:c.541C>A, NM_001143810.1:c.541C>A, NM_001143813.2:c.295C>A, NM_001143813.1:c.295C>A, NM_001143812.2:c.295C>A, NM_001143812.1:c.295C>A, NM_001143809.2:c.382C>A, NM_001143809.1:c.382C>A, NM_001143808.2:c.295C>A, NM_001143808.1:c.295C>A, NM_001143807.2:c.295C>A, NM_001143807.1:c.295C>A, NM_001143806.1:c.295C>A, NM_001143805.1:c.295C>A, NR_002832.2:n.404G>T, NR_033312.1:n.335G>T, NR_033314.1:n.404G>T, NR_033315.1:n.335G>T, NR_033313.1:n.335G>T, NM_001143815.1:c.295C>A, NP_733931.1:p.Gln99Lys, NP_733927.1:p.Gln107Lys, NP_001700.2:p.Gln99Lys, NP_733928.1:p.Gln99Lys, NP_733929.1:p.Gln99Lys, NP_733930.1:p.Gln114Lys, NP_001137288.1:p.Gln99Lys, NP_001137283.1:p.Gln99Lys, NP_001137286.1:p.Gln99Lys, NP_001137282.1:p.Gln181Lys, NP_001137285.1:p.Gln99Lys, NP_001137284.1:p.Gln99Lys, NP_001137281.1:p.Gln128Lys, NP_001137280.1:p.Gln99Lys, NP_001137279.1:p.Gln99Lys, NP_001137278.1:p.Gln99Lys, NP_001137277.1:p.Gln99Lys

Select item 14593270959.

rs1459327095 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:27657969 (GRCh38)
11:27679516 (GRCh37)
Canonical SPDI:: NC_000011.10:27657968:A:G
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.27657969A>G, NC_000011.9:g.27679516A>G, NG_011794.1:g.69090T>C, NM_170735.6:c.596T>C, NM_170735.5:c.596T>C, NM_170731.5:c.620T>C, NM_170731.4:c.620T>C, NM_001709.5:c.596T>C, NM_001709.4:c.596T>C, NM_170732.4:c.596T>C, NM_170733.4:c.596T>C, NM_170733.3:c.596T>C, NM_170734.4:c.641T>C, NM_170734.3:c.641T>C, NM_001143816.2:c.596T>C, NM_001143816.1:c.596T>C, NM_001143811.2:c.596T>C, NM_001143811.1:c.596T>C, NM_001143814.2:c.596T>C, NM_001143814.1:c.596T>C, NM_001143810.2:c.842T>C, NM_001143810.1:c.842T>C, NM_001143813.2:c.596T>C, NM_001143813.1:c.596T>C, NM_001143812.2:c.596T>C, NM_001143812.1:c.596T>C, NM_001143809.2:c.683T>C, NM_001143809.1:c.683T>C, NM_001143808.2:c.596T>C, NM_001143808.1:c.596T>C, NM_001143807.2:c.596T>C, NM_001143807.1:c.596T>C, NM_001143806.1:c.596T>C, NM_001143805.1:c.596T>C, NM_001143815.1:c.596T>C, NP_733931.1:p.Ile199Thr, NP_733927.1:p.Ile207Thr, NP_001700.2:p.Ile199Thr, NP_733928.1:p.Ile199Thr, NP_733929.1:p.Ile199Thr, NP_733930.1:p.Ile214Thr, NP_001137288.1:p.Ile199Thr, NP_001137283.1:p.Ile199Thr, NP_001137286.1:p.Ile199Thr, NP_001137282.1:p.Ile281Thr, NP_001137285.1:p.Ile199Thr, NP_001137284.1:p.Ile199Thr, NP_001137281.1:p.Ile228Thr, NP_001137280.1:p.Ile199Thr, NP_001137279.1:p.Ile199Thr, NP_001137278.1:p.Ile199Thr, NP_001137277.1:p.Ile199Thr

Select item 145904890110.

rs1459048901 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:27700992 (GRCh38)
11:27722539 (GRCh37)
Canonical SPDI:: NC_000011.10:27700991:A:C,NC_000011.10:27700991:A:G
Gene:: BDNF (Varview)
Functional Consequence:: synonymous_variant,5_prime_UTR_variant,intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
C=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.27700992A>C, NC_000011.10:g.27700992A>G, NC_000011.9:g.27722539A>C, NC_000011.9:g.27722539A>G, NG_011794.1:g.26067T>G, NG_011794.1:g.26067T>C, NM_001143811.2:c.-443T>G, NM_001143811.2:c.-443T>C, NM_001143811.1:c.-443T>G, NM_001143811.1:c.-443T>C, NM_001143810.2:c.-80T>G, NM_001143810.2:c.-80T>C, NM_001143810.1:c.-80T>G, NM_001143810.1:c.-80T>C, NM_001143809.2:c.45T>G, NM_001143809.2:c.45T>C, NM_001143809.1:c.45T>G, NM_001143809.1:c.45T>C, NM_001143808.2:c.-33T>G, NM_001143808.2:c.-33T>C, NM_001143808.1:c.-33T>G, NM_001143808.1:c.-33T>C

Select item 145160336411.

rs1451603364 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:27658411 (GRCh38)
11:27679958 (GRCh37)
Canonical SPDI:: NC_000011.10:27658410:C:T
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.27658411C>T, NC_000011.9:g.27679958C>T, NG_011794.1:g.68648G>A, NM_170735.6:c.154G>A, NM_170735.5:c.154G>A, NM_170731.5:c.178G>A, NM_170731.4:c.178G>A, NM_001709.5:c.154G>A, NM_001709.4:c.154G>A, NM_170732.4:c.154G>A, NM_170733.4:c.154G>A, NM_170733.3:c.154G>A, NM_170734.4:c.199G>A, NM_170734.3:c.199G>A, NM_001143816.2:c.154G>A, NM_001143816.1:c.154G>A, NM_001143811.2:c.154G>A, NM_001143811.1:c.154G>A, NM_001143814.2:c.154G>A, NM_001143814.1:c.154G>A, NM_001143810.2:c.400G>A, NM_001143810.1:c.400G>A, NM_001143813.2:c.154G>A, NM_001143813.1:c.154G>A, NM_001143812.2:c.154G>A, NM_001143812.1:c.154G>A, NM_001143809.2:c.241G>A, NM_001143809.1:c.241G>A, NM_001143808.2:c.154G>A, NM_001143808.1:c.154G>A, NM_001143807.2:c.154G>A, NM_001143807.1:c.154G>A, NM_001143806.1:c.154G>A, NM_001143805.1:c.154G>A, NR_002832.2:n.545C>T, NR_033312.1:n.476C>T, NR_033314.1:n.545C>T, NR_033315.1:n.476C>T, NR_033313.1:n.476C>T, NM_001143815.1:c.154G>A, NP_733931.1:p.Gly52Ser, NP_733927.1:p.Gly60Ser, NP_001700.2:p.Gly52Ser, NP_733928.1:p.Gly52Ser, NP_733929.1:p.Gly52Ser, NP_733930.1:p.Gly67Ser, NP_001137288.1:p.Gly52Ser, NP_001137283.1:p.Gly52Ser, NP_001137286.1:p.Gly52Ser, NP_001137282.1:p.Gly134Ser, NP_001137285.1:p.Gly52Ser, NP_001137284.1:p.Gly52Ser, NP_001137281.1:p.Gly81Ser, NP_001137280.1:p.Gly52Ser, NP_001137279.1:p.Gly52Ser, NP_001137278.1:p.Gly52Ser, NP_001137277.1:p.Gly52Ser

Select item 143282452412.

rs1432824524 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:27701014 (GRCh38)
11:27722561 (GRCh37)
Canonical SPDI:: NC_000011.10:27701013:C:T
Gene:: BDNF (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant,5_prime_UTR_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.27701014C>T, NC_000011.9:g.27722561C>T, NG_011794.1:g.26045G>A, NM_001143811.2:c.-465G>A, NM_001143811.1:c.-465G>A, NM_001143810.2:c.-102G>A, NM_001143810.1:c.-102G>A, NM_001143809.2:c.23G>A, NM_001143809.1:c.23G>A, NM_001143808.2:c.-55G>A, NM_001143808.1:c.-55G>A, NP_001137281.1:p.Cys8Tyr

Select item 143147567813.

rs1431475678 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:27658555 (GRCh38)
11:27680102 (GRCh37)
Canonical SPDI:: NC_000011.10:27658554:G:C
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.27658555G>C, NC_000011.9:g.27680102G>C, NG_011794.1:g.68504C>G, NM_170735.6:c.10C>G, NM_170735.5:c.10C>G, NM_170731.5:c.34C>G, NM_170731.4:c.34C>G, NM_001709.5:c.10C>G, NM_001709.4:c.10C>G, NM_170732.4:c.10C>G, NM_170733.4:c.10C>G, NM_170733.3:c.10C>G, NM_170734.4:c.55C>G, NM_170734.3:c.55C>G, NM_001143816.2:c.10C>G, NM_001143816.1:c.10C>G, NM_001143811.2:c.10C>G, NM_001143811.1:c.10C>G, NM_001143814.2:c.10C>G, NM_001143814.1:c.10C>G, NM_001143810.2:c.256C>G, NM_001143810.1:c.256C>G, NM_001143813.2:c.10C>G, NM_001143813.1:c.10C>G, NM_001143812.2:c.10C>G, NM_001143812.1:c.10C>G, NM_001143809.2:c.97C>G, NM_001143809.1:c.97C>G, NM_001143808.2:c.10C>G, NM_001143808.1:c.10C>G, NM_001143807.2:c.10C>G, NM_001143807.1:c.10C>G, NM_001143806.1:c.10C>G, NM_001143805.1:c.10C>G, NM_001143815.1:c.10C>G, NP_733931.1:p.Leu4Val, NP_733927.1:p.Leu12Val, NP_001700.2:p.Leu4Val, NP_733928.1:p.Leu4Val, NP_733929.1:p.Leu4Val, NP_733930.1:p.Leu19Val, NP_001137288.1:p.Leu4Val, NP_001137283.1:p.Leu4Val, NP_001137286.1:p.Leu4Val, NP_001137282.1:p.Leu86Val, NP_001137285.1:p.Leu4Val, NP_001137284.1:p.Leu4Val, NP_001137281.1:p.Leu33Val, NP_001137280.1:p.Leu4Val, NP_001137279.1:p.Leu4Val, NP_001137278.1:p.Leu4Val, NP_001137277.1:p.Leu4Val

Select item 143019300414.

rs1430193004 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:27657834 (GRCh38)
11:27679381 (GRCh37)
Canonical SPDI:: NC_000011.10:27657833:T:G
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.27657834T>G, NC_000011.9:g.27679381T>G, NG_011794.1:g.69225A>C, NM_170735.6:c.731A>C, NM_170735.5:c.731A>C, NM_170731.5:c.755A>C, NM_170731.4:c.755A>C, NM_001709.5:c.731A>C, NM_001709.4:c.731A>C, NM_170732.4:c.731A>C, NM_170733.4:c.731A>C, NM_170733.3:c.731A>C, NM_170734.4:c.776A>C, NM_170734.3:c.776A>C, NM_001143816.2:c.731A>C, NM_001143816.1:c.731A>C, NM_001143811.2:c.731A>C, NM_001143811.1:c.731A>C, NM_001143814.2:c.731A>C, NM_001143814.1:c.731A>C, NM_001143810.2:c.977A>C, NM_001143810.1:c.977A>C, NM_001143813.2:c.731A>C, NM_001143813.1:c.731A>C, NM_001143812.2:c.731A>C, NM_001143812.1:c.731A>C, NM_001143809.2:c.818A>C, NM_001143809.1:c.818A>C, NM_001143808.2:c.731A>C, NM_001143808.1:c.731A>C, NM_001143807.2:c.731A>C, NM_001143807.1:c.731A>C, NM_001143806.1:c.731A>C, NM_001143805.1:c.731A>C, NM_001143815.1:c.731A>C, NP_733931.1:p.Lys244Thr, NP_733927.1:p.Lys252Thr, NP_001700.2:p.Lys244Thr, NP_733928.1:p.Lys244Thr, NP_733929.1:p.Lys244Thr, NP_733930.1:p.Lys259Thr, NP_001137288.1:p.Lys244Thr, NP_001137283.1:p.Lys244Thr, NP_001137286.1:p.Lys244Thr, NP_001137282.1:p.Lys326Thr, NP_001137285.1:p.Lys244Thr, NP_001137284.1:p.Lys244Thr, NP_001137281.1:p.Lys273Thr, NP_001137280.1:p.Lys244Thr, NP_001137279.1:p.Lys244Thr, NP_001137278.1:p.Lys244Thr, NP_001137277.1:p.Lys244Thr

Select item 142703675915.

rs1427036759 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:27658181 (GRCh38)
11:27679728 (GRCh37)
Canonical SPDI:: NC_000011.10:27658180:G:A
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.27658181G>A, NC_000011.9:g.27679728G>A, NG_011794.1:g.68878C>T, NM_170735.6:c.384C>T, NM_170735.5:c.384C>T, NM_170731.5:c.408C>T, NM_170731.4:c.408C>T, NM_001709.5:c.384C>T, NM_001709.4:c.384C>T, NM_170732.4:c.384C>T, NM_170733.4:c.384C>T, NM_170733.3:c.384C>T, NM_170734.4:c.429C>T, NM_170734.3:c.429C>T, NM_001143816.2:c.384C>T, NM_001143816.1:c.384C>T, NM_001143811.2:c.384C>T, NM_001143811.1:c.384C>T, NM_001143814.2:c.384C>T, NM_001143814.1:c.384C>T, NM_001143810.2:c.630C>T, NM_001143810.1:c.630C>T, NM_001143813.2:c.384C>T, NM_001143813.1:c.384C>T, NM_001143812.2:c.384C>T, NM_001143812.1:c.384C>T, NM_001143809.2:c.471C>T, NM_001143809.1:c.471C>T, NM_001143808.2:c.384C>T, NM_001143808.1:c.384C>T, NM_001143807.2:c.384C>T, NM_001143807.1:c.384C>T, NM_001143806.1:c.384C>T, NM_001143805.1:c.384C>T, NM_001143815.1:c.384C>T

Select item 141521099116.

rs1415210991 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:27701003 (GRCh38)
11:27722550 (GRCh37)
Canonical SPDI:: NC_000011.10:27701002:G:C
Gene:: BDNF (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,genic_upstream_transcript_variant,intron_variant,missense_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.27701003G>C, NC_000011.9:g.27722550G>C, NG_011794.1:g.26056C>G, NM_001143811.2:c.-454C>G, NM_001143811.1:c.-454C>G, NM_001143810.2:c.-91C>G, NM_001143810.1:c.-91C>G, NM_001143809.2:c.34C>G, NM_001143809.1:c.34C>G, NM_001143808.2:c.-44C>G, NM_001143808.1:c.-44C>G, NP_001137281.1:p.Arg12Gly

Select item 141512585617.

rs1415125856 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:27658550 (GRCh38)
11:27680097 (GRCh37)
Canonical SPDI:: NC_000011.10:27658549:G:A
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000031/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.27658550G>A, NC_000011.9:g.27680097G>A, NG_011794.1:g.68509C>T, NM_170735.6:c.15C>T, NM_170735.5:c.15C>T, NM_170731.5:c.39C>T, NM_170731.4:c.39C>T, NM_001709.5:c.15C>T, NM_001709.4:c.15C>T, NM_170732.4:c.15C>T, NM_170733.4:c.15C>T, NM_170733.3:c.15C>T, NM_170734.4:c.60C>T, NM_170734.3:c.60C>T, NM_001143816.2:c.15C>T, NM_001143816.1:c.15C>T, NM_001143811.2:c.15C>T, NM_001143811.1:c.15C>T, NM_001143814.2:c.15C>T, NM_001143814.1:c.15C>T, NM_001143810.2:c.261C>T, NM_001143810.1:c.261C>T, NM_001143813.2:c.15C>T, NM_001143813.1:c.15C>T, NM_001143812.2:c.15C>T, NM_001143812.1:c.15C>T, NM_001143809.2:c.102C>T, NM_001143809.1:c.102C>T, NM_001143808.2:c.15C>T, NM_001143808.1:c.15C>T, NM_001143807.2:c.15C>T, NM_001143807.1:c.15C>T, NM_001143806.1:c.15C>T, NM_001143805.1:c.15C>T, NM_001143815.1:c.15C>T

Select item 140213946418.

rs1402139464 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:27701009 (GRCh38)
11:27722556 (GRCh37)
Canonical SPDI:: NC_000011.10:27701008:G:A,NC_000011.10:27701008:G:T
Gene:: BDNF (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.27701009G>A, NC_000011.10:g.27701009G>T, NC_000011.9:g.27722556G>A, NC_000011.9:g.27722556G>T, NG_011794.1:g.26050C>T, NG_011794.1:g.26050C>A, NM_001143811.2:c.-460C>T, NM_001143811.2:c.-460C>A, NM_001143811.1:c.-460C>T, NM_001143811.1:c.-460C>A, NM_001143810.2:c.-97C>T, NM_001143810.2:c.-97C>A, NM_001143810.1:c.-97C>T, NM_001143810.1:c.-97C>A, NM_001143809.2:c.28C>T, NM_001143809.2:c.28C>A, NM_001143809.1:c.28C>T, NM_001143809.1:c.28C>A, NM_001143808.2:c.-50C>T, NM_001143808.2:c.-50C>A, NM_001143808.1:c.-50C>T, NM_001143808.1:c.-50C>A, NP_001137281.1:p.Arg10Cys, NP_001137281.1:p.Arg10Ser

Select item 140184359419.

rs1401843594 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:27658327 (GRCh38)
11:27679874 (GRCh37)
Canonical SPDI:: NC_000011.10:27658326:T:C
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.27658327T>C, NC_000011.9:g.27679874T>C, NG_011794.1:g.68732A>G, NM_170735.6:c.238A>G, NM_170735.5:c.238A>G, NM_170731.5:c.262A>G, NM_170731.4:c.262A>G, NM_001709.5:c.238A>G, NM_001709.4:c.238A>G, NM_170732.4:c.238A>G, NM_170733.4:c.238A>G, NM_170733.3:c.238A>G, NM_170734.4:c.283A>G, NM_170734.3:c.283A>G, NM_001143816.2:c.238A>G, NM_001143816.1:c.238A>G, NM_001143811.2:c.238A>G, NM_001143811.1:c.238A>G, NM_001143814.2:c.238A>G, NM_001143814.1:c.238A>G, NM_001143810.2:c.484A>G, NM_001143810.1:c.484A>G, NM_001143813.2:c.238A>G, NM_001143813.1:c.238A>G, NM_001143812.2:c.238A>G, NM_001143812.1:c.238A>G, NM_001143809.2:c.325A>G, NM_001143809.1:c.325A>G, NM_001143808.2:c.238A>G, NM_001143808.1:c.238A>G, NM_001143807.2:c.238A>G, NM_001143807.1:c.238A>G, NM_001143806.1:c.238A>G, NM_001143805.1:c.238A>G, NR_002832.2:n.461T>C, NR_033312.1:n.392T>C, NR_033314.1:n.461T>C, NR_033315.1:n.392T>C, NR_033313.1:n.392T>C, NM_001143815.1:c.238A>G, NP_733931.1:p.Asn80Asp, NP_733927.1:p.Asn88Asp, NP_001700.2:p.Asn80Asp, NP_733928.1:p.Asn80Asp, NP_733929.1:p.Asn80Asp, NP_733930.1:p.Asn95Asp, NP_001137288.1:p.Asn80Asp, NP_001137283.1:p.Asn80Asp, NP_001137286.1:p.Asn80Asp, NP_001137282.1:p.Asn162Asp, NP_001137285.1:p.Asn80Asp, NP_001137284.1:p.Asn80Asp, NP_001137281.1:p.Asn109Asp, NP_001137280.1:p.Asn80Asp, NP_001137279.1:p.Asn80Asp, NP_001137278.1:p.Asn80Asp, NP_001137277.1:p.Asn80Asp

Select item 139174519920.

rs1391745199 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:27657830 (GRCh38)
11:27679377 (GRCh37)
Canonical SPDI:: NC_000011.10:27657829:C:T
Gene:: BDNF (Varview), BDNF-AS (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.27657830C>T, NC_000011.9:g.27679377C>T, NG_011794.1:g.69229G>A, NM_170735.6:c.735G>A, NM_170735.5:c.735G>A, NM_170731.5:c.759G>A, NM_170731.4:c.759G>A, NM_001709.5:c.735G>A, NM_001709.4:c.735G>A, NM_170732.4:c.735G>A, NM_170733.4:c.735G>A, NM_170733.3:c.735G>A, NM_170734.4:c.780G>A, NM_170734.3:c.780G>A, NM_001143816.2:c.735G>A, NM_001143816.1:c.735G>A, NM_001143811.2:c.735G>A, NM_001143811.1:c.735G>A, NM_001143814.2:c.735G>A, NM_001143814.1:c.735G>A, NM_001143810.2:c.981G>A, NM_001143810.1:c.981G>A, NM_001143813.2:c.735G>A, NM_001143813.1:c.735G>A, NM_001143812.2:c.735G>A, NM_001143812.1:c.735G>A, NM_001143809.2:c.822G>A, NM_001143809.1:c.822G>A, NM_001143808.2:c.735G>A, NM_001143808.1:c.735G>A, NM_001143807.2:c.735G>A, NM_001143807.1:c.735G>A, NM_001143806.1:c.735G>A, NM_001143805.1:c.735G>A, NM_001143815.1:c.735G>A

<< First< Prev

Page of 10

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 197

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity