U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Protein

Items: 1 to 20 of 163

1.

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

    2.

    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

      3.

      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

        4.

        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

          5.

          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

            6.

            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

              7.

              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

                8.

                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

                  9.

                  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

                    10.

                    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

                      11.

                      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

                        12.

                        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

                          13.

                          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

                            14.

                            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

                              15.

                              rs1386951839 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                11:27658358 (GRCh38)
                                11:27679905 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:27658357:C:T
                                Gene:
                                BDNF (Varview), BDNF-AS (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000008/2 (GnomAD_exomes)
                                HGVS:
                                NC_000011.10:g.27658358C>T, NC_000011.9:g.27679905C>T, NG_011794.1:g.68701G>A, NM_170735.6:c.207G>A, NM_170735.5:c.207G>A, NM_170731.5:c.231G>A, NM_170731.4:c.231G>A, NM_001709.5:c.207G>A, NM_001709.4:c.207G>A, NM_170732.4:c.207G>A, NM_170733.4:c.207G>A, NM_170733.3:c.207G>A, NM_170734.4:c.252G>A, NM_170734.3:c.252G>A, NM_001143816.2:c.207G>A, NM_001143816.1:c.207G>A, NM_001143811.2:c.207G>A, NM_001143811.1:c.207G>A, NM_001143814.2:c.207G>A, NM_001143814.1:c.207G>A, NM_001143810.2:c.453G>A, NM_001143810.1:c.453G>A, NM_001143813.2:c.207G>A, NM_001143813.1:c.207G>A, NM_001143812.2:c.207G>A, NM_001143812.1:c.207G>A, NM_001143809.2:c.294G>A, NM_001143809.1:c.294G>A, NM_001143808.2:c.207G>A, NM_001143808.1:c.207G>A, NM_001143807.2:c.207G>A, NM_001143807.1:c.207G>A, NM_001143806.1:c.207G>A, NM_001143805.1:c.207G>A, NR_002832.2:n.492C>T, NR_033312.1:n.423C>T, NR_033314.1:n.492C>T, NR_033315.1:n.423C>T, NR_033313.1:n.423C>T, NM_001143815.1:c.207G>A

                                16.

                                rs1384115118 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  11:27658036 (GRCh38)
                                  11:27679583 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:27658035:G:A
                                  Gene:
                                  BDNF (Varview), BDNF-AS (Varview)
                                  Functional Consequence:
                                  synonymous_variant,intron_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000011.10:g.27658036G>A, NC_000011.9:g.27679583G>A, NG_011794.1:g.69023C>T, NM_170735.6:c.529C>T, NM_170735.5:c.529C>T, NM_170731.5:c.553C>T, NM_170731.4:c.553C>T, NM_001709.5:c.529C>T, NM_001709.4:c.529C>T, NM_170732.4:c.529C>T, NM_170733.4:c.529C>T, NM_170733.3:c.529C>T, NM_170734.4:c.574C>T, NM_170734.3:c.574C>T, NM_001143816.2:c.529C>T, NM_001143816.1:c.529C>T, NM_001143811.2:c.529C>T, NM_001143811.1:c.529C>T, NM_001143814.2:c.529C>T, NM_001143814.1:c.529C>T, NM_001143810.2:c.775C>T, NM_001143810.1:c.775C>T, NM_001143813.2:c.529C>T, NM_001143813.1:c.529C>T, NM_001143812.2:c.529C>T, NM_001143812.1:c.529C>T, NM_001143809.2:c.616C>T, NM_001143809.1:c.616C>T, NM_001143808.2:c.529C>T, NM_001143808.1:c.529C>T, NM_001143807.2:c.529C>T, NM_001143807.1:c.529C>T, NM_001143806.1:c.529C>T, NM_001143805.1:c.529C>T, NM_001143815.1:c.529C>T

                                  17.

                                  rs1354925566 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>A,T [Show Flanks]
                                    Chromosome:
                                    11:27658051 (GRCh38)
                                    11:27679598 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:27658050:C:A,NC_000011.10:27658050:C:T
                                    Gene:
                                    BDNF (Varview), BDNF-AS (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,missense_variant,intron_variant
                                    HGVS:
                                    NC_000011.10:g.27658051C>A, NC_000011.10:g.27658051C>T, NC_000011.9:g.27679598C>A, NC_000011.9:g.27679598C>T, NG_011794.1:g.69008G>T, NG_011794.1:g.69008G>A, NM_170735.6:c.514G>T, NM_170735.6:c.514G>A, NM_170735.5:c.514G>T, NM_170735.5:c.514G>A, NM_170731.5:c.538G>T, NM_170731.5:c.538G>A, NM_170731.4:c.538G>T, NM_170731.4:c.538G>A, NM_001709.5:c.514G>T, NM_001709.5:c.514G>A, NM_001709.4:c.514G>T, NM_001709.4:c.514G>A, NM_170732.4:c.514G>T, NM_170732.4:c.514G>A, NM_170733.4:c.514G>T, NM_170733.4:c.514G>A, NM_170733.3:c.514G>T, NM_170733.3:c.514G>A, NM_170734.4:c.559G>T, NM_170734.4:c.559G>A, NM_170734.3:c.559G>T, NM_170734.3:c.559G>A, NM_001143816.2:c.514G>T, NM_001143816.2:c.514G>A, NM_001143816.1:c.514G>T, NM_001143816.1:c.514G>A, NM_001143811.2:c.514G>T, NM_001143811.2:c.514G>A, NM_001143811.1:c.514G>T, NM_001143811.1:c.514G>A, NM_001143814.2:c.514G>T, NM_001143814.2:c.514G>A, NM_001143814.1:c.514G>T, NM_001143814.1:c.514G>A, NM_001143810.2:c.760G>T, NM_001143810.2:c.760G>A, NM_001143810.1:c.760G>T, NM_001143810.1:c.760G>A, NM_001143813.2:c.514G>T, NM_001143813.2:c.514G>A, NM_001143813.1:c.514G>T, NM_001143813.1:c.514G>A, NM_001143812.2:c.514G>T, NM_001143812.2:c.514G>A, NM_001143812.1:c.514G>T, NM_001143812.1:c.514G>A, NM_001143809.2:c.601G>T, NM_001143809.2:c.601G>A, NM_001143809.1:c.601G>T, NM_001143809.1:c.601G>A, NM_001143808.2:c.514G>T, NM_001143808.2:c.514G>A, NM_001143808.1:c.514G>T, NM_001143808.1:c.514G>A, NM_001143807.2:c.514G>T, NM_001143807.2:c.514G>A, NM_001143807.1:c.514G>T, NM_001143807.1:c.514G>A, NM_001143806.1:c.514G>T, NM_001143806.1:c.514G>A, NM_001143805.1:c.514G>T, NM_001143805.1:c.514G>A, NM_001143815.1:c.514G>T, NM_001143815.1:c.514G>A, NP_733931.1:p.Val172Leu, NP_733931.1:p.Val172Ile, NP_733927.1:p.Val180Leu, NP_733927.1:p.Val180Ile, NP_001700.2:p.Val172Leu, NP_001700.2:p.Val172Ile, NP_733928.1:p.Val172Leu, NP_733928.1:p.Val172Ile, NP_733929.1:p.Val172Leu, NP_733929.1:p.Val172Ile, NP_733930.1:p.Val187Leu, NP_733930.1:p.Val187Ile, NP_001137288.1:p.Val172Leu, NP_001137288.1:p.Val172Ile, NP_001137283.1:p.Val172Leu, NP_001137283.1:p.Val172Ile, NP_001137286.1:p.Val172Leu, NP_001137286.1:p.Val172Ile, NP_001137282.1:p.Val254Leu, NP_001137282.1:p.Val254Ile, NP_001137285.1:p.Val172Leu, NP_001137285.1:p.Val172Ile, NP_001137284.1:p.Val172Leu, NP_001137284.1:p.Val172Ile, NP_001137281.1:p.Val201Leu, NP_001137281.1:p.Val201Ile, NP_001137280.1:p.Val172Leu, NP_001137280.1:p.Val172Ile, NP_001137279.1:p.Val172Leu, NP_001137279.1:p.Val172Ile, NP_001137278.1:p.Val172Leu, NP_001137278.1:p.Val172Ile, NP_001137277.1:p.Val172Leu, NP_001137277.1:p.Val172Ile

                                    18.

                                    rs1350515000 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      11:27658246 (GRCh38)
                                      11:27679793 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:27658245:G:A
                                      Gene:
                                      BDNF (Varview), BDNF-AS (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,non_coding_transcript_variant,missense_variant
                                      Validated:
                                      by frequency,by cluster
                                      MAF:
                                      A=0.000008/2 (GnomAD_exomes)
                                      HGVS:
                                      NC_000011.10:g.27658246G>A, NC_000011.9:g.27679793G>A, NG_011794.1:g.68813C>T, NM_170735.6:c.319C>T, NM_170735.5:c.319C>T, NM_170731.5:c.343C>T, NM_170731.4:c.343C>T, NM_001709.5:c.319C>T, NM_001709.4:c.319C>T, NM_170732.4:c.319C>T, NM_170733.4:c.319C>T, NM_170733.3:c.319C>T, NM_170734.4:c.364C>T, NM_170734.3:c.364C>T, NM_001143816.2:c.319C>T, NM_001143816.1:c.319C>T, NM_001143811.2:c.319C>T, NM_001143811.1:c.319C>T, NM_001143814.2:c.319C>T, NM_001143814.1:c.319C>T, NM_001143810.2:c.565C>T, NM_001143810.1:c.565C>T, NM_001143813.2:c.319C>T, NM_001143813.1:c.319C>T, NM_001143812.2:c.319C>T, NM_001143812.1:c.319C>T, NM_001143809.2:c.406C>T, NM_001143809.1:c.406C>T, NM_001143808.2:c.319C>T, NM_001143808.1:c.319C>T, NM_001143807.2:c.319C>T, NM_001143807.1:c.319C>T, NM_001143806.1:c.319C>T, NM_001143805.1:c.319C>T, NR_002832.2:n.380G>A, NR_033312.1:n.311G>A, NR_033314.1:n.380G>A, NR_033315.1:n.311G>A, NR_033313.1:n.311G>A, NM_001143815.1:c.319C>T, NP_733931.1:p.Leu107Phe, NP_733927.1:p.Leu115Phe, NP_001700.2:p.Leu107Phe, NP_733928.1:p.Leu107Phe, NP_733929.1:p.Leu107Phe, NP_733930.1:p.Leu122Phe, NP_001137288.1:p.Leu107Phe, NP_001137283.1:p.Leu107Phe, NP_001137286.1:p.Leu107Phe, NP_001137282.1:p.Leu189Phe, NP_001137285.1:p.Leu107Phe, NP_001137284.1:p.Leu107Phe, NP_001137281.1:p.Leu136Phe, NP_001137280.1:p.Leu107Phe, NP_001137279.1:p.Leu107Phe, NP_001137278.1:p.Leu107Phe, NP_001137277.1:p.Leu107Phe

                                      19.

                                      rs1349681470 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A [Show Flanks]
                                        Chromosome:
                                        11:27658333 (GRCh38)
                                        11:27679880 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:27658332:G:A
                                        Gene:
                                        BDNF (Varview), BDNF-AS (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,non_coding_transcript_variant,missense_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        A=0.000014/2 (GnomAD)
                                        HGVS:
                                        NC_000011.10:g.27658333G>A, NC_000011.9:g.27679880G>A, NG_011794.1:g.68726C>T, NM_170735.6:c.232C>T, NM_170735.5:c.232C>T, NM_170731.5:c.256C>T, NM_170731.4:c.256C>T, NM_001709.5:c.232C>T, NM_001709.4:c.232C>T, NM_170732.4:c.232C>T, NM_170733.4:c.232C>T, NM_170733.3:c.232C>T, NM_170734.4:c.277C>T, NM_170734.3:c.277C>T, NM_001143816.2:c.232C>T, NM_001143816.1:c.232C>T, NM_001143811.2:c.232C>T, NM_001143811.1:c.232C>T, NM_001143814.2:c.232C>T, NM_001143814.1:c.232C>T, NM_001143810.2:c.478C>T, NM_001143810.1:c.478C>T, NM_001143813.2:c.232C>T, NM_001143813.1:c.232C>T, NM_001143812.2:c.232C>T, NM_001143812.1:c.232C>T, NM_001143809.2:c.319C>T, NM_001143809.1:c.319C>T, NM_001143808.2:c.232C>T, NM_001143808.1:c.232C>T, NM_001143807.2:c.232C>T, NM_001143807.1:c.232C>T, NM_001143806.1:c.232C>T, NM_001143805.1:c.232C>T, NR_002832.2:n.467G>A, NR_033312.1:n.398G>A, NR_033314.1:n.467G>A, NR_033315.1:n.398G>A, NR_033313.1:n.398G>A, NM_001143815.1:c.232C>T, NP_733931.1:p.Arg78Trp, NP_733927.1:p.Arg86Trp, NP_001700.2:p.Arg78Trp, NP_733928.1:p.Arg78Trp, NP_733929.1:p.Arg78Trp, NP_733930.1:p.Arg93Trp, NP_001137288.1:p.Arg78Trp, NP_001137283.1:p.Arg78Trp, NP_001137286.1:p.Arg78Trp, NP_001137282.1:p.Arg160Trp, NP_001137285.1:p.Arg78Trp, NP_001137284.1:p.Arg78Trp, NP_001137281.1:p.Arg107Trp, NP_001137280.1:p.Arg78Trp, NP_001137279.1:p.Arg78Trp, NP_001137278.1:p.Arg78Trp, NP_001137277.1:p.Arg78Trp

                                        20.

                                        rs1339220115 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          11:27658119 (GRCh38)
                                          11:27679666 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:27658118:G:A
                                          Gene:
                                          BDNF (Varview), BDNF-AS (Varview)
                                          Functional Consequence:
                                          missense_variant,coding_sequence_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000004/1 (GnomAD_exomes)
                                          A=0.000004/1 (TOPMED)
                                          A=0.000007/1 (GnomAD)
                                          HGVS:
                                          NC_000011.10:g.27658119G>A, NC_000011.9:g.27679666G>A, NG_011794.1:g.68940C>T, NM_170735.6:c.446C>T, NM_170735.5:c.446C>T, NM_170731.5:c.470C>T, NM_170731.4:c.470C>T, NM_001709.5:c.446C>T, NM_001709.4:c.446C>T, NM_170732.4:c.446C>T, NM_170733.4:c.446C>T, NM_170733.3:c.446C>T, NM_170734.4:c.491C>T, NM_170734.3:c.491C>T, NM_001143816.2:c.446C>T, NM_001143816.1:c.446C>T, NM_001143811.2:c.446C>T, NM_001143811.1:c.446C>T, NM_001143814.2:c.446C>T, NM_001143814.1:c.446C>T, NM_001143810.2:c.692C>T, NM_001143810.1:c.692C>T, NM_001143813.2:c.446C>T, NM_001143813.1:c.446C>T, NM_001143812.2:c.446C>T, NM_001143812.1:c.446C>T, NM_001143809.2:c.533C>T, NM_001143809.1:c.533C>T, NM_001143808.2:c.446C>T, NM_001143808.1:c.446C>T, NM_001143807.2:c.446C>T, NM_001143807.1:c.446C>T, NM_001143806.1:c.446C>T, NM_001143805.1:c.446C>T, NM_001143815.1:c.446C>T, NP_733931.1:p.Thr149Met, NP_733927.1:p.Thr157Met, NP_001700.2:p.Thr149Met, NP_733928.1:p.Thr149Met, NP_733929.1:p.Thr149Met, NP_733930.1:p.Thr164Met, NP_001137288.1:p.Thr149Met, NP_001137283.1:p.Thr149Met, NP_001137286.1:p.Thr149Met, NP_001137282.1:p.Thr231Met, NP_001137285.1:p.Thr149Met, NP_001137284.1:p.Thr149Met, NP_001137281.1:p.Thr178Met, NP_001137280.1:p.Thr149Met, NP_001137279.1:p.Thr149Met, NP_001137278.1:p.Thr149Met, NP_001137277.1:p.Thr149Met

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity

                                          Clear Turn Off Turn On

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...