75256054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112073160-C-T

http://identifiers.org/hco/12/GRCh38#75256122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112073091-A-C

75256282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112072930-A-T

75256643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112072530-G-T

75256747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112072434-G-A

75257459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112071750-A-G

75257468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112071741-T-C

http://identifiers.org/hco/12/GRCh38#75257472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112071737-C-A

75257622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112071586-T-G

http://identifiers.org/hco/12/GRCh38#75257686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112071523-C-A

75257738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112071470-G-T

75257820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112071408-G-T

75257839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112071389-A-T

75257876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112071349-A-T

75257927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112071298-T-C

75258080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112071156-G-C

http://identifiers.org/hco/12/GRCh38#75258184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112071067-C-A

http://identifiers.org/hco/12/GRCh38#75258228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112071018-C-A

75258420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112070873-T-C

75258602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: non coding transcript exon variant
orthologous variants: 112070692-A-T

http://identifiers.org/hco/12/GRCh38#75258634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112070659-C-A

75258645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112070648-T-C

http://identifiers.org/hco/12/GRCh38#75258653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112070637-C-A

75258700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112070598-T-C

75258747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112070519-G-A

75258747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112070519-G-T

http://identifiers.org/hco/12/GRCh38#75259063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112070188-C-A

75259063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112070188-C-G

75259065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112070186-A-T

75259188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112069895-T-C

75259287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112069791-A-G

75259465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112069637-A-G

75259821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112069329-C-T

75259844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112069302-A-G

75260185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068986-A-G

75260294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068879-A-G

75260344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068828-G-A

75260344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068828-G-T

75260466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112068713-C-T

75260528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112068663-C-G

75260548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068644-C-T

http://identifiers.org/hco/12/GRCh38#75260559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112068634-C-A

75260574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 112068616-G-A

http://identifiers.org/hco/12/GRCh38#75260585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112068605-C-A

75260585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112068605-C-T

http://identifiers.org/hco/12/GRCh38#75261933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112068580-C-A

75262313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068236-C-T

75262362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068187-T-C

75262416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112068130-C-T

http://identifiers.org/hco/12/GRCh38#75266989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112066363-A-C

75267113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112066253-A-G

75267442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112065906-A-G

75267518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112065878-G-C

75267577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112065820-A-G

75267602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112065795-G-T

75267796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112065611-T-C

75267801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112065606-A-G

http://identifiers.org/hco/12/GRCh38#75267832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112065591-A-C

75268319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112063333-T-C

75268372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112063287-A-G

75268716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112062944-G-A

http://identifiers.org/hco/12/GRCh38#75268725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112062935-C-A

75268725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112062935-C-T

75268744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112062916-A-G

75268777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112062890-G-A

75268777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112062890-G-T

75272059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112059021-A-G

75272061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112059019-G-A

75272093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058987-T-C

75272105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058975-T-A

75272616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058880-T-A

75272651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058855-G-C

75272680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058826-A-T

75272703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058812-G-T

75272717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058803-G-C

75272803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058739-C-T

75272863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058677-C-G

75272864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058676-T-C

75272920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112058617-T-G

75273007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112057638-A-T

75273113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112057539-T-C

75273143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112057509-T-C

http://identifiers.org/hco/12/GRCh38#75273295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#112057289-C-A

75273464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112057116-C-T

75273580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112056997-T-G

75273711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112056859-T-G

75273715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112056855-A-G

75273945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112056626-A-T

75276708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053181-T-A

75276709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053180-A-G

http://identifiers.org/hco/12/GRCh38#75276747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112053137-C-A

75276754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053130-A-G

75276754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053130-A-T

75276760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053124-T-C

75276761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053123-A-G

75276763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053120-A-G

75276764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053119-A-T

75276817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053067-T-C

http://identifiers.org/hco/12/GRCh38#75276834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112053049-C-A

75276834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112053049-C-T

http://identifiers.org/hco/12/GRCh38#75276911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112052981-A-C

75276911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052981-A-G

75276954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052932-T-C

75277014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052874-A-G

75277068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052821-T-A

http://identifiers.org/hco/12/GRCh38#75277847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112052531-C-A

75277848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052530-C-T

75277883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052498-A-G

75277948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052433-A-G

75277970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052410-T-A

75277985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052395-T-C

75277991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052389-T-C

75277995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052385-A-G

75278004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052376-T-C

75278092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052317-G-A

75278092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052317-G-T

75278097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052315-G-A

75278097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052315-G-T

75278106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052306-A-G

75278150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052251-G-T

75278202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052223-C-T

75278220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052215-G-T

75278237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052198-C-T

75278299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052138-G-C

http://identifiers.org/hco/12/GRCh38#75278306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112052131-C-A

http://identifiers.org/hco/12/GRCh38#75278365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112052074-A-C

75278411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112052028-T-G

75278456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051986-G-T

http://identifiers.org/hco/12/GRCh38#75278484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112051958-A-C

75278487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051955-G-A

75278487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051955-G-T

75278533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051913-A-G

http://identifiers.org/hco/12/GRCh38#75278542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112051904-C-A

75278542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051904-C-T

75278559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051887-A-G

75278592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051831-A-G

75278597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051826-T-G

75278645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051759-T-C

75278645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051759-T-G

75278649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051755-A-G

75278686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051706-A-G

75278686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051706-A-T

75278706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051672-T-G

75278713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051665-T-G

75278793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051602-T-A

75278793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051602-T-C

75278813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051583-G-A

75278813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051583-G-T

75278839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051559-T-C

http://identifiers.org/hco/12/GRCh38#75278843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112051555-C-A

75278843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051555-C-T

75278867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051531-G-A

75278867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051531-G-C

75278874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051523-T-C

75278876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051521-T-A

75278876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051521-T-C

75278876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051521-T-G

75278877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051520-G-A

75278896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051501-C-G

75278896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051501-C-T

75278901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051496-A-G

75278904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051493-G-A

75278904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051493-G-T

75279062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051335-T-C

75279080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051316-T-C

75279123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051274-T-A

75279123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051274-T-C

75279129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051268-T-C

http://identifiers.org/hco/12/GRCh38#75279163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112051234-C-A

75279175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051222-A-G

75279176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051221-T-C

http://identifiers.org/hco/12/GRCh38#75279197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112051199-A-C

75279228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051168-A-G

75279229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051167-T-C

75279232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051164-C-T

75279242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051156-G-A

75279346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051056-T-A

75279346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112051056-T-C

75279416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050993-A-G

75279432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050977-G-C

75279672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050721-T-G

75279687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050706-A-T

75279811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050596-G-T

75279852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050558-C-G

75279977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050504-T-C

75280011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050470-T-C

75280085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050397-T-C

75280197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050190-T-C

75280206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112050181-T-C

75280389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112049897-C-T

75280905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112048859-T-C

http://identifiers.org/hco/12/GRCh38#75280914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112048851-A-C

75281204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112048280-G-A

75281213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112048266-A-G

75281234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112048245-A-G

75281258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112048221-G-T

75281486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112048005-T-C

http://identifiers.org/hco/12/GRCh38#75281601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112047820-A-C

75281773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112047662-T-C

75281853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112047469-G-T

75282128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112047216-G-C

75282128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112047216-G-T

75282301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112047046-A-G

75282353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 112046994-C-T

75282913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046752-A-G

75282914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046751-C-G

75282978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046691-G-C

http://identifiers.org/hco/12/GRCh38#75282987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112046682-C-A

75283009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046662-C-T

75283103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046536-A-G

75283137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046524-T-C

75283204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046447-A-G

http://identifiers.org/hco/12/GRCh38#75283272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112046377-C-A

75283323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046327-C-T

75283437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112046220-T-C

http://identifiers.org/hco/12/GRCh38#75283938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112046043-C-A

75283994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112045953-T-C

75283998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112045949-T-G

75284205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112045712-T-A

75284548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044718-A-G

75284615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044670-C-T

75284892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044371-A-G

75284972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044295-A-G

75285025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044242-T-A

75285025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044242-T-C

75285039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044228-A-G

75285108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112044112-A-G

http://identifiers.org/hco/12/GRCh38#75285160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112044064-C-A

75285536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112043564-T-C

75285724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112043118-T-C

75285800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042936-C-T

75285809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042927-C-T

75285844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042896-A-T

75286270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042504-A-G

75286293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042481-G-A

75286317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042456-C-T

75286335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042438-G-A

75286366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042399-A-G

75286555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042269-T-A

75286583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042247-T-A

75286604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042231-A-G

75286649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042186-A-G

http://identifiers.org/hco/12/GRCh38#75286722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112042119-C-A

75286813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112042024-T-A

75288207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112041245-G-A

75288224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112041228-T-C

75288243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112041209-G-A

75288368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112041074-C-T

75288371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112041071-C-T

75288386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112041056-T-C

75288557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040908-G-A

75288672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040809-G-A

http://identifiers.org/hco/12/GRCh38#75288732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112040767-A-C

http://identifiers.org/hco/12/GRCh38#75288919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112040599-C-A

75288996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040549-T-G

75289027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040517-T-G

75289033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040516-A-T

75289107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040461-C-T

75289255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040288-C-G

75289357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040193-T-C

75289409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040140-A-G

http://identifiers.org/hco/12/GRCh38#75289475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112040070-C-A

75289475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112040070-C-G

75289587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039971-T-C

75289628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039930-G-T

http://identifiers.org/hco/12/GRCh38#75289783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112039775-A-C

75289783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 112039775-A-T

http://identifiers.org/hco/12/GRCh38#75289835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112039723-C-A

75289835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039723-C-T

http://identifiers.org/hco/12/GRCh38#75289846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112039712-C-A

75289846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039712-C-T

75289859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039699-A-G

75289877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039681-T-G

http://identifiers.org/hco/12/GRCh38#75289901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112039657-A-C

75289908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039650-G-A

75289908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039650-G-T

75289936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039625-T-A

75290049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039509-T-G

http://identifiers.org/hco/12/GRCh38#75290078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112039480-A-C

75290113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039444-C-T

75290275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039287-C-T

75290442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039150-A-G

75290442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039150-A-T

75290530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039063-A-G

75290593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112039009-C-T

http://identifiers.org/hco/12/GRCh38#75292554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112036266-A-C

75292613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112036195-G-A

75292613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112036195-G-T

75292698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112036095-G-A

75292698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112036095-G-C

75292839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112036045-A-G

http://identifiers.org/hco/12/GRCh38#75292892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112035997-A-C

75292931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035959-T-C

75293156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035752-T-C

75293173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035735-T-A

75293201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035709-A-G

http://identifiers.org/hco/12/GRCh38#75293211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112035699-C-A

http://identifiers.org/hco/12/GRCh38#75293357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112035555-A-C

75293383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035529-G-C

75293383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035529-G-T

75293402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035497-C-T

75293417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035483-A-G

75293417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112035483-A-T

75293727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112034742-G-T

75293841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112034630-T-A

75296998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112034025-A-G

75297007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112034016-T-C

75297105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112033924-C-T

75297261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112033767-G-A

75297279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112033749-G-A

75297465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112033571-T-A

75297657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112033290-T-C

75297717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112033052-C-T

75297873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032896-C-T

http://identifiers.org/hco/12/GRCh38#75298029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112032785-A-C

75298047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032763-T-C

75298052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032758-T-C

75298240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032656-G-T

75298241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032655-T-C

http://identifiers.org/hco/12/GRCh38#75298297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112032608-C-A

75298328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032573-T-A

75298328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032573-T-C

75298328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032573-T-G

75298354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032552-T-C

75298354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032552-T-G

75298361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032545-G-T

75298365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032541-T-C

http://identifiers.org/hco/12/GRCh38#75298376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112032530-C-A

75298382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032526-A-G

75298382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032526-A-T

http://identifiers.org/hco/12/GRCh38#75298388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#112032520-C-A

75298388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032520-C-T

75298454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032431-G-T

75298466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032426-T-C

75298466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032426-T-G

75298474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032418-A-G

75298474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40769
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112032418-A-T