44793159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116825177-T-C

44793479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116824933-T-A

44793479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116824933-T-C

44793507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116824905-G-A

44793507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116824905-G-C

44794010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116824434-C-T

44794759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823791-T-C

44794913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823642-A-G

44794966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823609-G-A

44795103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823463-T-C

44795113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823453-T-C

44795121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823445-A-G

44795199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823349-A-G

44795414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823139-G-A

44795478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: non coding transcript exon variant
orthologous variants: 116823075-C-T

44797243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819423-A-T

44797261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819407-T-C

44797286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819377-T-C

44797290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819375-T-C

44797415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819247-C-T

44797443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819219-G-A

44797443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819219-G-T

44797486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116819176-T-C

44797825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116818879-T-C

http://identifiers.org/hco/10/GRCh38#44797919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116818782-C-A

44797941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116818760-G-A

44798058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116818689-G-A

44798256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116818428-T-A

44798256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116818428-T-C

44798338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116818320-T-G

44801689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806958-T-C

44802001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806664-T-C

44802023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806643-A-G

44802199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806467-G-A

44802406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806264-C-T

44802567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806101-A-G

44802571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806097-A-G

44802582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806086-T-A

44802607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116806061-G-A

44802832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116805494-T-C

44802870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116805452-T-A

44802870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116805452-T-C

44803232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116805155-C-T

44803405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116804989-G-T

44803416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116804975-A-G

44803704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116804759-G-T

44803895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116804585-C-T

44803997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116804483-A-G

44804199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116804234-G-A

44804199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116804234-G-T

44806609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803908-C-T

44806626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803891-C-T

44806677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803841-A-G

44807118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803280-T-A

44807118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803280-T-C

44807136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803262-A-G

44807154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803244-G-A

44807154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803244-G-T

http://identifiers.org/hco/10/GRCh38#44807174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116803224-C-A

44807174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803224-C-T

44807293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803104-T-A

44807293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803104-T-C

44807293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803104-T-G

44807304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803093-G-A

44807304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803093-G-C

44807304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803093-G-T

44807316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803081-A-G

44807339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803058-T-C

44807365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803032-A-G

44807369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116803028-T-C

http://identifiers.org/hco/10/GRCh38#44807398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116802999-C-A

44807432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116802980-A-G

44807479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116802935-C-G

http://identifiers.org/hco/10/GRCh38#44807588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116802857-C-A

http://identifiers.org/hco/10/GRCh38#44807840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116802674-C-A

44807840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116802674-C-T

44807851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116802663-G-T

http://identifiers.org/hco/10/GRCh38#44808092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116801274-C-A

44808092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116801274-C-G

44808506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116800906-A-G

44810804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116800821-C-T

44810826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116800796-A-G

44810852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116800770-T-A

44810852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116800770-T-C

44810873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116800748-T-G

44811218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116800434-A-G

44811221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116800431-G-T

44811269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116800373-T-A

http://identifiers.org/hco/10/GRCh38#44811746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116798395-C-A

44811815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798322-T-C

44811836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798301-G-A

44811836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798301-G-T

http://identifiers.org/hco/10/GRCh38#44811879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116798261-C-A

44811919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798221-T-C

44811985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798156-A-G

44812005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798136-T-G

44812026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798115-T-A

44812026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798115-T-G

44812062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798086-C-T

44812141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116798020-A-G

44812248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116797936-A-G

http://identifiers.org/hco/10/GRCh38#44812254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116797930-C-A

44812275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116797909-T-C

http://identifiers.org/hco/10/GRCh38#44812432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116797783-C-A

44812432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116797783-C-T

44812543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116797269-C-G

44813963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116796481-T-C

44814240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116795875-A-T

44814410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116795688-C-T

44814693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116795460-G-A

44815024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116795204-A-G

44815160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116795097-T-A

44815945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794924-T-G

44816011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794861-G-A

44816025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794847-G-C

http://identifiers.org/hco/10/GRCh38#44816047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116794826-C-A

44816125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794747-T-C

http://identifiers.org/hco/10/GRCh38#44816232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116794659-A-C

44816267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794630-T-C

44816304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794594-C-T

44816314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794584-T-C

44816375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116794527-A-G

44816888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793753-A-G

44816928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793714-A-G

44817044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793616-T-G

44817047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793613-G-A

44817072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793588-C-T

44817088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793572-T-C

44817093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793561-T-C

44817282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793427-G-A

http://identifiers.org/hco/10/GRCh38#44817574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116793145-A-C

44817607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793123-G-A

44817607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793123-G-T

44817628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793102-T-C

44817637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793093-T-C

44817646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793084-G-A

44817646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793084-G-C

44817646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793084-G-T

44817662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116793068-A-G

44817883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116792907-G-C

44817893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116792897-A-G

44817920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116792871-G-T

http://identifiers.org/hco/10/GRCh38#44817968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116792827-C-A

44817968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116792827-C-G

44817975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116792823-G-A

44818315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116792464-G-A

44818428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116791961-G-T

44818524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116791872-C-G

44820091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116790840-A-G

http://identifiers.org/hco/10/GRCh38#44820200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116790746-A-C

44820200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116790746-A-G

http://identifiers.org/hco/10/GRCh38#44820249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116790697-A-C

44820261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116790675-A-G

44820293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116790643-C-T

44820487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116789149-C-G

44821209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788949-C-T

http://identifiers.org/hco/10/GRCh38#44821324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116788838-C-A

44821324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788838-C-G

44821508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788653-G-A

http://identifiers.org/hco/10/GRCh38#44821630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116788513-C-A

44821630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788513-C-T

44821975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788218-C-T

44822060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788149-A-G

44822060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788149-A-T

44822163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788037-G-T

44822180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116788017-C-T

44822204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787995-T-C

44822235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787964-T-C

44822274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787931-C-G

44822274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787931-C-T

44822283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787922-C-G

44822331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787869-G-A

44822409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787788-A-T

44822452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787749-C-T

44822474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787727-A-T

44822479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787722-C-T

44822538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787658-T-C

44822538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787658-T-G

44822642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787573-T-C

44822788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787306-G-A

44822904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787194-T-C

http://identifiers.org/hco/10/GRCh38#44822915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116787183-C-A

44822915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787183-C-T

44823004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787099-G-A

http://identifiers.org/hco/10/GRCh38#44823047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116787057-C-A

44823051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787053-A-G

44823077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116787029-T-A

http://identifiers.org/hco/10/GRCh38#44823170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116786947-C-A

44823170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786947-C-T

44823417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786732-A-T

44823424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786725-C-G

44823424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786725-C-T

44823560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786591-G-A

44823700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786358-G-A

44823700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786358-G-C

44823734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786238-G-A

44823746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786226-T-C

44823756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786216-G-A

44823757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116786215-T-C

44823955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116785997-A-T

http://identifiers.org/hco/10/GRCh38#44824056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116785889-A-C

44824860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116785071-G-A

44825035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116785150-G-A

44825224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116785322-A-G

http://identifiers.org/hco/10/GRCh38#44828173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116775057-C-A

44828520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774611-G-C

44828627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774502-C-G

44828685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774443-G-T

44828759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774360-T-A

44828759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774360-T-C

44828795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774321-T-A

44828809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774307-G-A

44828848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116774263-T-C

44829225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116773303-G-A

44829271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116773254-G-A

http://identifiers.org/hco/10/GRCh38#44829279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116773247-C-A

44829397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116773123-G-A

44829397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116773123-G-C

44829486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116773068-T-C

44829552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116773028-G-A

44829641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116772909-C-T

44829665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116772885-C-G

http://identifiers.org/hco/10/GRCh38#44829700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116772851-C-A

44830053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116772492-G-A

44830053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116772492-G-C

44830068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116772477-A-G

44834564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771873-T-C

44834575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771862-G-T

44834584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771857-A-G

44834770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771649-A-G

44834770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771649-A-T

44834787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771636-G-T

http://identifiers.org/hco/10/GRCh38#44834813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116771609-C-A

44835039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771404-C-T

44835107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771333-A-T

44835117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771323-T-C

http://identifiers.org/hco/10/GRCh38#44835128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116771312-C-A

44835128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771312-C-T

http://identifiers.org/hco/10/GRCh38#44835197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116771266-C-A

44835197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771266-C-T

44835204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116771259-C-T

44835390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116771083-G-A

44835390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116771083-G-T

44835430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116771043-C-G

44835477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116770993-A-G

44835687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116770783-C-T

44836025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116770461-A-G

44836025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116770461-A-T

44836159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116770337-T-A

44836174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116770322-T-A

44836174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116770322-T-C

44844778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116763906-A-G

44845382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116763429-A-G

44845433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116763373-A-T

44845501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116763324-T-A

44845692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116763143-T-C

44845894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116762867-C-T

44845930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116762842-G-T

44846196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116762561-G-T

44855847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116755508-G-T

44856045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116755314-A-G

http://identifiers.org/hco/10/GRCh38#44856099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116755270-A-C

44856099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116755270-A-T

44856347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116755035-A-G

44856509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116754896-C-G

44856656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116754797-T-C

44856792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116754662-T-C

44856855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116753915-G-A

44856863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116753907-G-A

44856863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116753907-G-T

44856878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116753892-C-T

44857048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116753740-A-G

44857405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116752570-C-T

44857466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116752513-A-G

44857501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116752477-C-T

44857634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116752348-G-A

44857653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116752329-G-A

44857782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116752216-A-T

44857788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116752211-G-T

44857817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116752182-G-A

44860306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750873-C-T

44860307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750872-G-A

44860318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750861-T-C

44860375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750794-T-C

http://identifiers.org/hco/10/GRCh38#44860789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116750442-C-A

44860789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750442-C-T

44860935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750298-T-C

44861039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750221-G-A

44861039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750221-G-T

44861264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116750012-A-T

44861640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116749690-C-G

44861871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116749488-T-C

http://identifiers.org/hco/10/GRCh38#44861982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116749383-A-C

http://identifiers.org/hco/10/GRCh38#44861999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116749365-C-A

44862007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116749357-G-A

44862126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116749251-G-T

44862365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116749114-T-A

44862482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116749027-C-G

44862482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116749027-C-T

http://identifiers.org/hco/10/GRCh38#44862587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116748932-C-A

44862704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116748801-T-C

44862704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116748801-T-G

44863112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746564-A-T

44863201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746465-G-C

44863219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746452-T-C

http://identifiers.org/hco/10/GRCh38#44863229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116746442-C-A

44863255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746418-T-C

44863257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746416-G-A

http://identifiers.org/hco/10/GRCh38#44863353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116746316-C-A

44863353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746316-C-T

44863433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746279-T-C

44863438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746274-T-C

44863532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116746182-C-G

44864021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116745788-G-C

44864164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116745652-G-A

44864363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116745497-C-T

44864373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116745487-A-G

44864836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116745012-C-T

44864853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116744995-C-T

44865034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116744828-G-C

http://identifiers.org/hco/10/GRCh38#44865293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116744576-C-A

44865334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116744527-G-A

44865636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116744289-G-A

44865675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116744252-G-A

44866150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116743615-T-C

44866185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116743592-A-G

44866208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116743575-C-G

44866332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116743460-G-A

44866876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116743211-G-A

44866979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116743113-T-G

44871421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116740616-G-A

44871446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116740591-T-C

44871598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116740456-T-C

44871880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116740148-C-T

http://identifiers.org/hco/10/GRCh38#44871919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116740111-C-A

44871997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116740037-T-C

44872388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116739863-T-C

44872391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116739860-A-T

44872645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116739606-G-C

http://identifiers.org/hco/10/GRCh38#44872685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116739567-C-A

44872848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116739453-G-T

http://identifiers.org/hco/10/GRCh38#44872911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116739377-A-C

44872949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116739340-A-G

44873460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116738195-A-G

44873696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116737933-T-C

44873866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116737765-T-C

44874003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116737661-C-T

44874024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116737639-C-T

44874151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737557-T-G

44874161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737547-T-C

44874195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737513-C-G

44874351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737341-C-T

44874410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737282-T-C

44874410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737282-T-G

44874576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737140-G-A

http://identifiers.org/hco/10/GRCh38#44874589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116737127-C-A

44874589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737127-C-T

44877590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116737557-T-C

44881434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116732183-T-G

44881590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116732010-C-T

44881704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731943-C-T

44881751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731896-A-G

44881780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731867-G-A

44881789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731858-G-A

44881836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731807-G-A

44881854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731790-C-T

http://identifiers.org/hco/10/GRCh38#44881867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116731777-A-C

44881867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731777-A-G

http://identifiers.org/hco/10/GRCh38#44882002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116731645-C-A

44882297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731459-A-G

44882332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731432-G-A

44882356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731393-T-C

44882364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731385-C-G

44882402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731349-G-C

44882450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116731289-T-C

http://identifiers.org/hco/10/GRCh38#44883024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116730812-C-A

44883076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116730761-C-T

44883079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116730758-C-T

44883098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116730737-C-T

http://identifiers.org/hco/10/GRCh38#44886744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116726847-C-A

44886810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726764-G-T

44886902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726652-A-T

44886953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726593-G-A

44886953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726593-G-T

44887042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726504-G-A

44887062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726499-A-G

44887195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726389-C-T

44887219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726365-T-C

44887319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726261-G-A

44887319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726261-G-C

44888342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116724835-C-G

44888810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116717115-T-A

44888871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116717056-T-C

44888871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116717056-T-G

44888930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716939-A-G

http://identifiers.org/hco/10/GRCh38#44889191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116716682-C-A

44891258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716370-C-T

44891580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716092-C-T

44893107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713831-T-C

44893135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713803-A-G

44893200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713737-G-T

44893247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713697-A-G

44893261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713680-T-C

44893601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713437-T-C

44893601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713437-T-G

44893726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713312-C-T

44893891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713148-C-T

44894121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116712995-G-A

44894179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116712937-G-A

44895311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711721-A-G

44895350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711682-T-G

44895391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711641-T-G

44895399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711633-G-A

44895399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711633-G-C

http://identifiers.org/hco/10/GRCh38#44895460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116711580-C-A

44895586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711506-T-C

44895644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711446-G-A

44895746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116711317-C-T

44897540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116703135-G-A

44897578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116703127-C-G

44897591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116703116-G-A

44897599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116703106-T-C

44897692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702894-C-T

44897931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702554-G-C

44897995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702487-G-A

44898022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702465-G-C

44898133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702352-G-A

44898134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702351-A-G

44898215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702276-A-G

44898293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702200-G-A

44898748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116702071-C-G

44902422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116701563-G-T

44902466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116701527-A-G

44902576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116701408-T-A

http://identifiers.org/hco/10/GRCh38#44902785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116700666-A-C

44902911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116700523-C-T

44903008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116700416-C-T

44903011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116700413-G-C

44903109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116700313-C-T

44903201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116700213-G-A

44903540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699995-T-C

http://identifiers.org/hco/10/GRCh38#44903785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116699788-C-A

44903945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699628-G-A

44904098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699481-G-C

44904201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699386-T-C

44904442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699327-T-C

44904784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699173-G-A

44904786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699171-T-C

44904786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699171-T-G

44904821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699139-G-A

http://identifiers.org/hco/10/GRCh38#44904918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116699036-C-A

44904930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116699024-A-T

44906187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116697960-G-A

44906712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116697377-C-T

http://identifiers.org/hco/10/GRCh38#44906845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116697236-C-A

44906856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116697228-G-A

44906856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116697228-G-T

44906900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116697186-T-C

44906901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116697185-G-T

44906950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116697139-G-A

44906950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116697139-G-C

44906950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116697139-G-T

44906955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116697131-A-G

44907088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116696984-A-G

44907862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116696612-C-T

44907952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116696531-G-A

44908136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116696367-G-A

44908136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116696367-G-C

http://identifiers.org/hco/10/GRCh38#44908733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116695815-C-A

44908844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116695671-G-A

44908844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116695671-G-T

44908895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116695598-A-G

44909157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116695365-C-T

44909557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694981-T-C

44910482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694563-A-T

44910496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694549-G-C

44910557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694484-C-T

http://identifiers.org/hco/10/GRCh38#44910763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116694283-C-A

44910798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694269-C-T

44910805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694262-T-A

44910814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694252-G-A

44910922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694151-C-G

44910922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694151-C-T

44910951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694122-C-T

44910960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694113-T-C

44911005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116694052-A-G

44911071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693999-G-A

44911072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693998-A-G

44911075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693995-T-C

http://identifiers.org/hco/10/GRCh38#44911090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116693977-C-A

44911093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693974-G-A

44911093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693974-G-T

44911106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693961-G-A

44911106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693961-G-C

http://identifiers.org/hco/10/GRCh38#44911194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116693870-A-C

44911254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693806-T-G

44911335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693726-G-A

44911335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693726-G-T

44911364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693697-G-T

44911469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693580-T-A

44911469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693580-T-G

44911471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693578-T-G

44911625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693423-C-G

44911625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693423-C-T

44911630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693418-G-C

44911630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693418-G-T

44911665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693383-G-A

44911665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693383-G-C

44911665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693383-G-T

http://identifiers.org/hco/10/GRCh38#44911729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116693319-C-A

44911729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693319-C-G

44911729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693319-C-T

44911797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693253-T-C

http://identifiers.org/hco/10/GRCh38#44912329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116692786-C-A

44912448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692669-C-G

44912645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692476-C-T

44912683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692455-G-A

44912777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692378-G-A

44912903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692264-G-C

44912962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692209-G-T

44913121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692129-T-C

44913135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692116-G-A

44913208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692074-C-T

44913243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692014-T-G

44913272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116691971-C-T

44913458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691815-A-G

44913461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691812-C-G

http://identifiers.org/hco/10/GRCh38#44913494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116691791-A-C

44913494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691791-A-G

44913559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691726-G-T

http://identifiers.org/hco/10/GRCh38#44916223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116690253-C-A

44916567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689673-T-A

44916715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689541-C-T

44916787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689487-T-C

44916847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689427-C-T

44917417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116688991-G-A

http://identifiers.org/hco/10/GRCh38#44917422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116688986-A-C

44917422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116688986-A-T

44919790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680106-T-C

http://identifiers.org/hco/10/GRCh38#44919804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116680092-A-C

http://identifiers.org/hco/10/GRCh38#44919853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116680043-C-A

44919853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680043-C-T

44919874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680023-T-C

44919897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680000-T-A

44919897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680000-T-C

44919897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680000-T-G

44919924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116679986-T-C

44919924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116679986-T-G

44927811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679110-G-A

44927811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679110-G-T

44927814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679107-G-A

44927814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679107-G-T

44927815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679106-T-C

44927833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679089-A-G

44927833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679089-A-T

44927875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679049-G-C

44927890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679033-G-A

44927896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679027-T-C

44927988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116678935-G-A

44927988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116678935-G-T

44928006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678922-G-A

44928006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678922-G-T

44928011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678917-T-C

http://identifiers.org/hco/10/GRCh38#44928082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116678849-C-A

44928082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678849-C-T

44928108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678824-G-A

44928109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678823-G-A

44928109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678823-G-T

44928675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678509-C-T

44928679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678505-C-T

44929080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678242-G-A

44929093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678230-T-G

http://identifiers.org/hco/10/GRCh38#44929466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116677931-C-A

44929466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677931-C-G

44929466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677931-C-T

44929515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677888-T-C

44929542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677860-G-A

44929565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677837-G-A

http://identifiers.org/hco/10/GRCh38#44929569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116677833-C-A

44929569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677833-C-T

44929818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677679-G-A

44929818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677679-G-C

44929818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677679-G-T

44929844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677662-C-T

44930313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677308-T-C

44930387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677231-G-A

44930428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677188-C-T

44930683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676984-G-A

44930750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676927-T-C

44930846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676827-G-A

44930846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676827-G-C

44930910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676754-T-C

44931012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676658-G-A

44931230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676476-G-A

44931231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676475-G-A

44931500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676103-G-A

44931500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676103-G-T

44931592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675896-C-G

44931703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675640-T-C

44931708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675636-G-T

44931714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675630-G-A

44931714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675630-G-C

44931714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675630-G-T

44931736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675607-G-C

44931736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675607-G-T

44931752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675591-G-A

44931752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675591-G-T

http://identifiers.org/hco/10/GRCh38#44931760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116675583-C-A

44931760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675583-C-T

44931768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675575-G-A

44931768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675575-G-T

44931858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675511-T-G

44931859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675510-G-A

44931859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675510-G-T

44931892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675457-C-T

44931893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675456-A-G

44931894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675455-T-C

44931937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675413-G-A

44931962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675389-G-A

44931962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675389-G-T

44931964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675387-G-A

44932092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675256-C-T

44932208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675149-T-A

44932208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675149-T-C

http://identifiers.org/hco/10/GRCh38#44932538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116674901-C-A

44932570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674881-C-T

http://identifiers.org/hco/10/GRCh38#44932616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116674823-C-A

44932616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674823-C-T

44932639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674798-G-A

44932644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674793-T-C

44932878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116674570-G-A

44933227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116674304-A-T

http://identifiers.org/hco/10/GRCh38#44933490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116674082-C-A

44933490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674082-C-T

44933521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674033-G-A

44933521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674033-G-T

http://identifiers.org/hco/10/GRCh38#44933561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116673991-C-A

44933561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673991-C-T

http://identifiers.org/hco/10/GRCh38#44933570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116673980-C-A

44933570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673980-C-T

44933572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673978-T-C

44933644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116673898-C-T

http://identifiers.org/hco/10/GRCh38#44933657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116673885-C-A

44933659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116673883-G-T

44933789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673752-G-A

44933789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673752-G-C

44933831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673707-G-C

44933831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673707-G-T

44933903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673656-G-A

44933903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673656-G-T

44933964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673607-G-A

44934022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673551-G-A

44934234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673369-A-G

http://identifiers.org/hco/10/GRCh38#44934551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672594-C-A

44934551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672594-C-T

44934568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672577-G-T

44934571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672574-G-T

44934577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672568-C-G

44934581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672564-T-C

44934600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672549-G-A

44934600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672549-G-T

44934602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672547-C-T

44934603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672546-T-A

44934603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672546-T-C

44934636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672509-G-T

http://identifiers.org/hco/10/GRCh38#44934719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672425-C-A

http://identifiers.org/hco/10/GRCh38#44934769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672375-A-C

44934853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116672291-T-C

44934853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116672291-T-G

http://identifiers.org/hco/10/GRCh38#44934973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672171-C-A

44934973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116672171-C-T

44934995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116672149-G-A

44935064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116672080-C-T

44935226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671911-T-C

44935240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671910-G-A

44935240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671910-G-C

http://identifiers.org/hco/10/GRCh38#44935252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671898-C-A

44935288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671862-G-A

44935318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671835-G-T

44935368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671792-T-C

http://identifiers.org/hco/10/GRCh38#44935372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671788-C-A

44935416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671763-G-A

44935416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671763-G-T

44935428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671751-G-A

http://identifiers.org/hco/10/GRCh38#44935432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671747-C-A

44935459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671720-A-G

44935459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671720-A-T

44935506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671691-T-A

44935506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671691-T-G

http://identifiers.org/hco/10/GRCh38#44935549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671631-C-A

44935549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671631-C-T

44935575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671602-T-C

44935719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671494-G-A

44935719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671494-G-T

44935849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671328-T-C

44935861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671307-A-G

44935887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671254-G-A

44935887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671254-G-T

44935898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671243-G-A

44935898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671243-G-T

44935916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671225-A-G

44935927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671212-G-A

44935927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671212-G-T

http://identifiers.org/hco/10/GRCh38#44935977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671160-C-A

44935977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671160-C-T

http://identifiers.org/hco/10/GRCh38#44935978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671159-A-C

44936057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671086-G-T

44936066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671077-G-A

44936066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671077-G-T

44936078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671065-C-T

44936089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671054-G-C

44936282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116670882-A-G

44936321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116670847-G-T

44936361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116670801-A-G

44936402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116670771-C-T

http://identifiers.org/hco/10/GRCh38#44936453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116670679-C-A

44936478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116670654-G-A

http://identifiers.org/hco/10/GRCh38#44936489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116670644-C-A

44936527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116670614-C-T

http://identifiers.org/hco/10/GRCh38#44936655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116670469-C-A

44936655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116670469-C-T

44947846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660095-C-T

44947908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116660040-C-T

44948071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116659881-T-C

44948479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116659601-A-G

44948597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116659505-C-T

44949066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658724-T-C

44949075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658715-T-C

44949300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658502-C-T

44949488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116657900-G-T

44949589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116657812-T-C

44949676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657737-G-A

44949883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657528-T-C

44950477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656794-C-G

44950477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656794-C-T

44950647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656653-C-T

44950721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656577-C-T

44951339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656368-C-T

44951340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656367-G-A

44951528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656212-T-A

44951562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656179-A-G

44951899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116655919-G-A

44952557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116655065-A-G

44952614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116654921-C-G

http://identifiers.org/hco/10/GRCh38#44953126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116654549-C-A

44953126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116654549-C-T

44953603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116654101-A-G

44953713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653940-G-T

44953983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653727-G-A

44953998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653713-C-T

44954278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653482-T-C

44954305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653455-T-A

44954478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653309-T-C

44954556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653240-C-T

44954557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653239-G-A

44955447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652487-G-T

44955453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652481-T-C

44955495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116652439-A-G

44955621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116652336-T-C

44958284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652122-A-G

44958777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116651656-A-G

44958828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116651592-C-T

http://identifiers.org/hco/10/GRCh38#44958829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116651591-A-C

http://identifiers.org/hco/10/GRCh38#44958858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116651563-C-A

44958858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116651563-C-T

44958969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116651453-A-G

44958981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116651441-T-C

http://identifiers.org/hco/10/GRCh38#44959043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116651411-C-A

44959064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116651390-T-C

44959115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116651348-T-C

44959133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116651332-G-T

44959142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116651323-A-T

44959165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116651299-T-G

http://identifiers.org/hco/10/GRCh38#44959173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116651289-C-A

44959173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116651289-C-T

http://identifiers.org/hco/10/GRCh38#44959311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116651176-C-A

44959464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116651030-T-C