109166002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41592441-G-T

109182642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41573391-A-G

109182994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41573056-G-A

109183143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41572916-A-G

109183178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41572884-G-A

109183580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41572262-C-T

109184031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41570405-A-G

109184038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41570398-G-A

109184038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41570398-G-T

109184051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41570385-G-C

109184092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 41570344-G-T

http://identifiers.org/hco/6/GRCh38#109184120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41570321-C-A

109184127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570314-G-T

http://identifiers.org/hco/6/GRCh38#109184138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41570303-C-A

109184138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570303-C-G

109184138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570303-C-T

109184511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41569573-T-A

109184511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41569573-T-C

109185512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41569188-C-T

109185737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41569006-A-G

109185951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568589-T-G

109185994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568499-A-G

http://identifiers.org/hco/6/GRCh38#109186005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41568489-A-C

109186071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568435-G-A

109186117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568400-A-T

109186448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568069-G-A

109187001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41567030-C-G

109187244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41566812-A-G

109187424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41566635-A-G

109187568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41566521-G-A

109187568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41566521-G-T

http://identifiers.org/hco/6/GRCh38#109187592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41566497-C-A

http://identifiers.org/hco/6/GRCh38#109187598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41566491-C-A

http://identifiers.org/hco/6/GRCh38#109187626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41566463-C-A

109187743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41566348-T-C

http://identifiers.org/hco/6/GRCh38#109187757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41566334-C-A

http://identifiers.org/hco/6/GRCh38#109187792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41566290-C-A

109187792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41566290-C-T

109188229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41565877-G-A

http://identifiers.org/hco/6/GRCh38#109189365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41565426-A-C

109189410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41565412-G-T

109189941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41564735-T-C

http://identifiers.org/hco/6/GRCh38#109190227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41564435-C-A

109195655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41559458-A-G

http://identifiers.org/hco/6/GRCh38#109196370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41559395-A-C

109196370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41559395-A-G

109196370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41559395-A-T

http://identifiers.org/hco/6/GRCh38#109196451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41559322-C-A

109196484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 41559275-G-A

109196484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 41559275-G-T

109196503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41559256-G-A

109196503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41559256-G-T

109196603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41559156-G-A

109196605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41559154-A-G

109196619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41559140-A-G

http://identifiers.org/hco/6/GRCh38#109196674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41558537-A-C

109196674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41558537-A-G

109196815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41558016-T-C

109196951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41557882-T-C

109196953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41557880-G-A

109196991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41557843-T-C

109197045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41557814-G-A

109197056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41557803-G-A

109197175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41557684-C-T

109197211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41557648-A-G

109197250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41557609-G-A

http://identifiers.org/hco/6/GRCh38#109197253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41557606-C-A

109197253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41557606-C-T

http://identifiers.org/hco/6/GRCh38#109197301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41557582-C-A

109197301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41557582-C-T

109198023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41556782-C-G

http://identifiers.org/hco/6/GRCh38#109198222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41556440-C-A

109198222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41556440-C-T

http://identifiers.org/hco/6/GRCh38#109198338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41556367-C-A

http://identifiers.org/hco/6/GRCh38#109198501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41556221-C-A

http://identifiers.org/hco/6/GRCh38#109198502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41556220-C-A

109198502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41556220-C-T

http://identifiers.org/hco/6/GRCh38#109198669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41555469-C-A

109198669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41555469-C-T

109198681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41555457-A-G

109198681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41555457-A-T

http://identifiers.org/hco/6/GRCh38#109198750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41555402-A-C

109198861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41555315-T-G

http://identifiers.org/hco/6/GRCh38#109199366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41555043-A-C

109199471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41554955-T-C

http://identifiers.org/hco/6/GRCh38#109199485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41554941-C-A

109199485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41554941-C-T

109199502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41554920-T-C

109199640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41554784-G-A

109199670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41554754-G-A

109199722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41554706-T-C

109201976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41552210-G-A

109202229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551948-T-C

109202237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551940-C-T

109202466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551778-A-G

109203460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551197-A-T

http://identifiers.org/hco/6/GRCh38#109203513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41551144-C-A

109203541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551121-G-A

http://identifiers.org/hco/6/GRCh38#109203586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41551079-C-A

109203595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551070-G-T

109203604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551062-A-G

109203604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41551062-A-T

109203707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41549960-C-T

109203763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41549904-A-G

109203804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41549863-T-C

http://identifiers.org/hco/6/GRCh38#109203822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41549845-C-A

109203879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549788-T-A

109203879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549788-T-C

109203880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549787-G-A

109203890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549777-T-C

109203914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549753-G-T

109203935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549731-G-A

http://identifiers.org/hco/6/GRCh38#109203941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41549725-C-A

109203941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549725-C-T

109203942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549724-A-G

http://identifiers.org/hco/6/GRCh38#109203979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41549708-C-A

109203979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549708-C-G

109203979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549708-C-T

109204137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549570-C-T

109204386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41549035-T-G

109204462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548960-G-A

109204524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548768-C-G

109204524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548768-C-T

109204536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548736-C-T

109204603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548637-T-C

109204662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548586-C-T

109204886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548375-G-A

109205288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548105-G-A

109205289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41548104-G-T

http://identifiers.org/hco/6/GRCh38#109206219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41542902-C-A

109206248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542877-A-G

109206249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542876-G-T

109206274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542845-T-C

109206443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41542699-A-G

109206443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41542699-A-T

109206476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542666-A-G

109206476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542666-A-T

http://identifiers.org/hco/6/GRCh38#109206500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41542636-C-A

109206508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542628-A-T

109206634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542475-A-G

109206793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542386-C-T

109206850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542333-G-A

109206850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542333-G-T

109206969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41542213-C-T

http://identifiers.org/hco/6/GRCh38#109214753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41541862-C-A

109214843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41541765-C-T

109214976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41541607-C-G

109214993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41541590-G-T

109215209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41541407-A-G

http://identifiers.org/hco/6/GRCh38#109215461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41541242-C-A

109215835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41540694-T-C

109215835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41540694-T-G

109215875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41540655-G-A

http://identifiers.org/hco/6/GRCh38#109215941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41540626-A-C

109216232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41540486-G-T

109216289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41540431-T-G

109216869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41539916-C-T

http://identifiers.org/hco/6/GRCh38#109216892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41539891-C-A

109217094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41539544-T-G

http://identifiers.org/hco/6/GRCh38#109217185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41539230-C-A

http://identifiers.org/hco/6/GRCh38#109217200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41539204-C-A

109217200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41539204-C-T

109217243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41539164-G-A

109217243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41539164-G-C

109217243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41539164-G-T

http://identifiers.org/hco/6/GRCh38#109217257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41539150-C-A

109217257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41539150-C-G

http://identifiers.org/hco/6/GRCh38#109217484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41538945-C-A

109217911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41538566-A-G

109217977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41538508-G-A

109218028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41538483-A-G

109218211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41538293-G-T

109218749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41537866-T-C

109218901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41537749-G-A

109218928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41537722-C-T

109223531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41533888-C-G

109223633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41533796-C-T

109223707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41533743-A-G

109225352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41533561-C-T

http://identifiers.org/hco/6/GRCh38#109225390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41533522-C-A

109225397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41533515-C-T

http://identifiers.org/hco/6/GRCh38#109225710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41533187-C-A

109225796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41533121-C-G

109225993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532944-T-G

109226139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532715-C-G

109226166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532680-G-T

109226234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532622-T-C

109226451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532428-A-G

109226451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532428-A-T

http://identifiers.org/hco/6/GRCh38#109226573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41532319-A-C

109226573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41532319-A-G

http://identifiers.org/hco/6/GRCh38#109226706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41532214-C-A

109226743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532181-T-A

109226745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532179-A-G

109226745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532179-A-T

109226748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41532176-G-T

http://identifiers.org/hco/6/GRCh38#109226773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41532151-C-A

109227090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531541-G-T

109227102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531529-G-A

109227102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531529-G-T

http://identifiers.org/hco/6/GRCh38#109227111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41531520-C-A

109227111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531520-C-G

109227142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531492-G-A

109227144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531490-G-A

http://identifiers.org/hco/6/GRCh38#109227165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41531469-C-A

109227165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531469-C-G

109227274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41531351-T-G

109227280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41531345-T-C

109227297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41531310-T-A

109227297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41531310-T-G

109227521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531064-T-C

http://identifiers.org/hco/6/GRCh38#109227569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41531016-A-C

109227569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41531016-A-G

http://identifiers.org/hco/6/GRCh38#109227614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41530971-C-A

109227621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41530964-A-G

109227627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41530958-G-A

109227627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41530958-G-C

109227627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41530958-G-T

109228411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41529518-A-T

109228417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41529512-G-A

109228503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41529426-G-A

109228517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41529412-T-G

109228858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41529121-T-C

109229164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528838-C-T

109229780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528579-G-A

109229784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528575-G-A

109229816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528555-T-A

109229870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528502-G-A

109230015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528370-A-G

109230071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528318-T-C

http://identifiers.org/hco/6/GRCh38#109230262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41528146-C-A

109230262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41528146-C-T

109231926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41526279-C-G

109232044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41526236-C-T

109232108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41526196-T-C

109239189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41523273-T-C

http://identifiers.org/hco/6/GRCh38#109239213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41523255-C-A

109239213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41523255-C-T

109239349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41523122-G-A

109239427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41523044-G-A

109239427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41523044-G-T

http://identifiers.org/hco/6/GRCh38#109239499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41522972-C-A

109239499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41522972-C-T

109239561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41522917-T-A

109240716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41522670-G-A

109241885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41521350-A-G

109242126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41520746-A-G

109242129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41520743-G-A

109242129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41520743-G-C

109242136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41520736-T-C

109242142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41520728-C-T

109242217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41520654-T-C

109242217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41520654-T-G

109242236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41520635-A-G

109242308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 41520563-T-C

http://identifiers.org/hco/6/GRCh38#109243008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41519905-C-A

109251501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518776-G-A

109251529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518748-C-T

109251707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518568-A-G

109251762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518509-G-A

109251762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518509-G-T

109251876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518392-T-C

109251913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518355-A-G

109251991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518281-G-A

109251991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41518281-G-T

109252240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41517982-G-T

109252480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41517746-T-C

http://identifiers.org/hco/6/GRCh38#109252518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41517704-A-C

109252638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41517604-T-G

109252899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41515510-C-T

109253031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41515387-T-G

109253116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41515303-C-T

109253144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41515277-C-T

109253217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41515198-C-T

http://identifiers.org/hco/6/GRCh38#109254342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41513433-C-A

109254342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41513433-C-T

109254359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41513386-A-G

http://identifiers.org/hco/6/GRCh38#109254412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41513322-C-A

http://identifiers.org/hco/6/GRCh38#109254429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41513305-C-A

http://identifiers.org/hco/6/GRCh38#109254634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41513100-A-C

109254634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41513100-A-G

109254642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41513092-C-G

109255176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41512398-G-C

109255176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41512398-G-T

http://identifiers.org/hco/6/GRCh38#109255277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41512290-A-C

109255277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41512290-A-G

109255418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41512179-T-C

http://identifiers.org/hco/6/GRCh38#109255481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41512116-C-A

http://identifiers.org/hco/6/GRCh38#109255512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41512085-A-C

http://identifiers.org/hco/6/GRCh38#109255565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41512033-A-C

109255565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41512033-A-G

http://identifiers.org/hco/6/GRCh38#109255621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41511992-C-A

109255963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41511815-C-G

109256433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41511424-T-C

109256442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41511415-T-C

109256745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41511160-C-T

http://identifiers.org/hco/6/GRCh38#109257009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41510623-C-A

109257009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510623-C-T

http://identifiers.org/hco/6/GRCh38#109257019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41510613-C-A

109257019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510613-C-G

http://identifiers.org/hco/6/GRCh38#109257021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41510611-C-A

109257021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510611-C-T

109257032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510600-G-A

109257058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510590-C-G

109257062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510586-C-T

109257094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510552-T-C

109257117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510530-C-G

109257117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510530-C-T

109257493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41510250-A-G

109257697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41510039-G-T

109257752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41509984-A-G

109257909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41509824-G-T

109258345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41509618-A-G

109259109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41508561-T-C

109259522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41508244-C-T

109259593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41508173-G-T

109259611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41508149-A-G

109260759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41507348-C-T

109260840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41507294-G-A

109260991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41507147-T-C

109261049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41506939-T-C

109261460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41506462-C-T

http://identifiers.org/hco/6/GRCh38#109261480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41506431-A-C

109261997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41506038-G-A

109261997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41506038-G-C

109262142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41505898-A-G

109262142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41505898-A-T

109262214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41505861-T-C

109262214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41505861-T-G

109262812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41504644-C-T

109263386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41504115-G-A

109263386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41504115-G-T

109264809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41503287-A-G

109264848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41503248-T-C

109264898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41503198-G-A

109264966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41503130-G-A

109265019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41503088-T-C

109265021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41503086-A-G

109265037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41503070-A-G

109265037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41503070-A-T

109265351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41502513-T-C

109265557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41502328-A-G

109265621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41502294-C-T

109265691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41502220-C-T

109265878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41502043-C-T

109265993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41501929-C-T

http://identifiers.org/hco/6/GRCh38#109266026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41501646-C-A

109266200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41501499-G-A

109266364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41501392-C-G

109266545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41501234-C-G

109266993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41501150-C-T

109267272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500913-C-T

109267274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500911-G-A

109267653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500824-A-G

109267663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500814-G-A

109267737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500740-T-C

109267765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500712-A-T

109267779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500698-T-C

109269513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41500015-G-A

109269745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499808-C-G

109269805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499758-G-A

http://identifiers.org/hco/6/GRCh38#109269894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41499687-C-A

109269894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499687-C-T

109269929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499652-T-G

109269934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499647-G-T

109269941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499640-A-G

http://identifiers.org/hco/6/GRCh38#109269961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41499590-A-C

109269967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499584-T-C

http://identifiers.org/hco/6/GRCh38#109269976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41499575-C-A

109269976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499575-C-G

109269976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499575-C-T

109270019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41499532-T-G

109270031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41499520-T-C

109270031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41499520-T-G

109270066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41499485-A-G

109270131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41499420-G-A

109270131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41499420-G-T

http://identifiers.org/hco/6/GRCh38#109270196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41499355-A-C

http://identifiers.org/hco/6/GRCh38#109270207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41499345-A-C

109270216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41499336-C-T

http://identifiers.org/hco/6/GRCh38#109270312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41499245-C-A

http://identifiers.org/hco/6/GRCh38#109270328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41499232-C-A

109281511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41492885-G-A

109281732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41492713-A-G

http://identifiers.org/hco/6/GRCh38#109281786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41492673-C-A

109282175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41492326-G-A

109282208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41492299-G-A

109282208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41492299-G-T

109282312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41492199-T-C

109282539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41492007-T-C

109282598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41491947-G-A

109283905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41491356-T-C

109284061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41491239-C-T

109284095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41491206-C-T

109284178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41491139-A-G

http://identifiers.org/hco/6/GRCh38#109284238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41491099-A-C

109284344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41491005-G-A

109284353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490996-A-G

109284359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490990-G-A

109284371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490978-G-A

109284371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490978-G-T

http://identifiers.org/hco/6/GRCh38#109284380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41490969-C-A

109284380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490969-C-T

http://identifiers.org/hco/6/GRCh38#109284510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41490843-C-A

109284510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41490843-C-T

109284562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41490791-A-G

109284625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490734-G-A

109284625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490734-G-T

109284655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490658-G-T

109284862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490406-C-G

109284909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41490370-G-T

http://identifiers.org/hco/6/GRCh38#109285338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41489987-C-A

109285497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41489806-A-G

http://identifiers.org/hco/6/GRCh38#109285532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41489760-C-A

109285593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41489681-G-A

109285593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41489681-G-T

109285644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489630-G-A

109285770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489507-A-G

109285809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489472-G-A

109285908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489391-A-T

109285924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489375-G-A

109286032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41489280-A-T

109286035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489277-G-T

109286136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489141-A-G

109286146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489131-G-A

109286146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489131-G-T

109286156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489122-G-T

http://identifiers.org/hco/6/GRCh38#109286194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41489084-C-A

109286194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489084-C-T

109286246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41489029-C-T

109286387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41488895-G-A

109286506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41488776-A-G

109286545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41488738-A-G

109286553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41488730-T-C

109287063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41485029-T-C

109287152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41484943-G-A

109287193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41484916-T-A

109287254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41484876-G-A

109287481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41484672-G-A

109293895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41483089-A-G

http://identifiers.org/hco/6/GRCh38#109294229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41482776-C-A

109294229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41482776-C-T

109294255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41482754-A-G

109294260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41482749-G-A

109294355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41482669-G-A

http://identifiers.org/hco/6/GRCh38#109294498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41482509-C-A

109294501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41482506-G-C

109294519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41482485-A-G

http://identifiers.org/hco/6/GRCh38#109294639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41482395-C-A

109294639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41482395-C-T

109295246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41481657-G-A

109295289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41481611-T-C

109295607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41481130-T-C

109295661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41481076-G-T

109295680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41481057-A-G

109295776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41480973-A-G

109295798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41480959-A-G

109295824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41480933-C-T

109295903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41480866-A-G

109295994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41480792-G-T

109296436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41479123-A-G

http://identifiers.org/hco/6/GRCh38#109296619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41478964-C-A

109296694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41478886-G-A

109296987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41478659-G-T

109296997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41478649-A-G

109297341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41478445-A-G

109297906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41477932-C-T

109297952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41477884-A-G

109298153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41477749-G-C

http://identifiers.org/hco/6/GRCh38#109298500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41476144-A-C

109298523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41476120-T-C

109298794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41475851-C-T

109298914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41475712-T-C

109300094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474687-A-G

109300094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474687-A-T

109300147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474632-T-A

109300150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474629-G-T

109300151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474628-G-A

109300151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474628-G-C

http://identifiers.org/hco/6/GRCh38#109300570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41474217-A-C

109300570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474217-A-G

109300699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474102-C-T

109300741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41474067-C-T

http://identifiers.org/hco/6/GRCh38#109301121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41473343-C-A

109301341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41473120-C-T

109301451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41473037-C-T

109301890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41472056-G-A

109301890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41472056-G-C

109301953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41471996-C-G

109302007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41471946-A-G

109302064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41471889-G-A

109302250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41471758-C-T

109302276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41471726-T-C

109302386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41471627-A-G

109304873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41466660-T-A

109304886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41466648-C-G

109304887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41466647-T-G

109305188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41466260-T-C

109305819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41465823-G-A

109305819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41465823-G-T

109305821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41465821-A-G

109306036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41465630-T-A

http://identifiers.org/hco/6/GRCh38#109306098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41465568-C-A

109306326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41465339-A-T

109306348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41465316-G-A

109306348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41465316-G-C

109306449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41464806-A-G

109306566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41464699-G-A

http://identifiers.org/hco/6/GRCh38#109306688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41464501-A-C

109306838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41464368-G-C

109307141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41464140-T-G

http://identifiers.org/hco/6/GRCh38#109307801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41463621-A-C

109307816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41463604-G-C

109307838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41463578-C-T

http://identifiers.org/hco/6/GRCh38#109307858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41463558-A-C

109307858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41463558-A-G

109307861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41463555-A-T

http://identifiers.org/hco/6/GRCh38#109307957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41463464-C-A

109308044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41463377-T-C

109308147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41463284-T-C

109308272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41463181-G-A

109308272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41463181-G-T

109308344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41463109-A-G

109308348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41463105-G-A

http://identifiers.org/hco/6/GRCh38#109308349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41463104-C-A

109308349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41463104-C-T

109308578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41462883-T-G

109308582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41462879-T-C

109308701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41462773-C-T

http://identifiers.org/hco/6/GRCh38#109309254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41462623-C-A

109309254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41462623-C-T

http://identifiers.org/hco/6/GRCh38#109309284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41462600-C-A

109309685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41462214-A-G

109309748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41462154-A-G

109312048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41460854-T-C

109312098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41460806-A-T

109312377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41460527-C-T

109312617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41459610-T-C

109312632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41459595-A-G

109312632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41459595-A-T

109312763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41459479-G-A

109313179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41459123-T-C

109313203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41459099-A-G

109313897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41457538-A-G

109314134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41457311-G-A

109314134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41457311-G-C

109314139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41457306-T-C

109314226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41457219-G-A

109314348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41457098-G-A

http://identifiers.org/hco/6/GRCh38#109314358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41457088-C-A

109314437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41457042-G-T

109315314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41456323-G-T

109315511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41456144-A-G

109315599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41456097-C-T

109316723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41455352-C-T

109318047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41453450-C-T

109318204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41453309-T-C

109318573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41452947-A-G

109318820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41452774-G-T

109318827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41452767-G-C

109319018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41452425-C-T

109319097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41452355-A-G

109319322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41452156-G-A

109319383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41452089-C-T

109320032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41451510-A-G

109320116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41451425-T-C

109323018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41449318-C-T

109323317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41448647-G-A

109323407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41448562-G-A

109323818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41448279-C-T

109323863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41448237-A-G

109329104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41445845-G-A

http://identifiers.org/hco/6/GRCh38#109329179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41445776-C-A

109329200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41445756-C-T

109332053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41442013-A-G

109332219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441904-G-A

109332242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441875-C-T

109332253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441868-C-T

109332276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441840-C-T

109332295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441823-G-T

109332387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441769-G-C

http://identifiers.org/hco/6/GRCh38#109332423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41441731-C-A

109332423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441731-C-T

109332446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441706-C-T

109332478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441678-C-G

109332478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441678-C-T

109332622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441508-C-T

109332669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41441461-C-T

109333155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41441064-C-T

109333338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41440894-C-T

109334634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41439066-G-A

109336055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41437551-G-A

http://identifiers.org/hco/6/GRCh38#109336160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41437459-C-A

109336160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41437459-C-T

109336161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41437457-G-A

109336285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41437339-A-G

109336290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41437334-A-G

109336351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41437271-T-C

http://identifiers.org/hco/6/GRCh38#109336353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41437269-C-A

109336353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41437269-C-T

109336474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 41437148-A-G

109336497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 41437125-A-G

109336645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41436994-T-A

109336645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41436994-T-C

109336661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41436978-C-T

109337444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41432764-G-T

109337519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41432730-A-G

109337567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41432698-C-T

109337575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41432690-G-A

109337575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41432690-G-T

http://identifiers.org/hco/6/GRCh38#109337609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41432666-C-A

109338427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41432156-C-T

109338660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41431934-G-A

109338660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41431934-G-C

109338660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41431934-G-T

109338704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41431909-G-T

109338773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41431705-C-G

109339121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41431175-T-G

109339311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41430993-T-C

109339621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41430647-A-G

109339621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41430647-A-T

109339703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41430611-T-C

109340730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41429680-T-A

109340984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41429480-A-G

109341058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41429394-T-C

109341474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41429033-G-A

109341553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41428933-C-G

109342325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41428533-A-G

109342352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41428508-G-A

http://identifiers.org/hco/6/GRCh38#109342455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41428408-A-C

109342455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41428408-A-G

http://identifiers.org/hco/6/GRCh38#109342637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41428252-C-A

109343478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41427447-A-G

109343664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41427253-T-C

109343710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41427207-A-G

109343756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41427153-C-T

http://identifiers.org/hco/6/GRCh38#109343851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41427036-C-A

109343900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41427004-T-G

http://identifiers.org/hco/6/GRCh38#109343948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41426964-C-A

109344293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41426638-G-A

109345575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41424914-T-C

109345575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41424914-T-G

109346862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41424003-T-C

109347093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41423795-A-G

http://identifiers.org/hco/6/GRCh38#109347094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41423794-A-C

109347100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41423788-A-T

109348333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41423097-G-A

109348362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41423067-A-G

109348472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41422952-C-G

109348475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41422949-C-T

109348514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: non coding transcript exon variant
orthologous variants: 41422910-C-T

109351528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41418977-A-G

109351718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41418805-G-A

109351740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41418783-A-T

109351878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41418645-C-T

109352200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41418338-T-G

109352204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41418334-G-A

109354202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41416187-G-A

109354202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41416187-G-T

109354354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41415993-G-T

109354386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41415970-A-G

109354456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41415894-T-C