2689496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 3 prime UTR variant
orthologous variants: 74561569-C-T

2689733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 3 prime UTR variant
orthologous variants: 74561305-A-G

2690522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 3 prime UTR variant
orthologous variants: 74560514-C-T

2690637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74560388-T-C

2690637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74560388-T-G

2690638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74560387-G-T

2690854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74560173-G-A

2691582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74558995-G-A

2691582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74558995-G-T

2691931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558624-G-A

2691931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558624-G-C

2691931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558624-G-T

2692263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558347-G-A

2692263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558347-G-C

2692263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558347-G-T

2692325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74558290-C-T

2692423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74558200-C-T

2692509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558117-G-A

2692509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74558117-G-T

http://identifiers.org/hco/17/GRCh38#2692543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74558082-C-A

2692587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74558033-T-G

http://identifiers.org/hco/17/GRCh38#2692936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74557703-C-A

2692936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557703-C-T

2692942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557702-A-G

2692942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557702-A-T

http://identifiers.org/hco/17/GRCh38#2693024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74557648-C-A

2693024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557648-C-T

2693336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557501-C-T

2693687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557321-G-A

2693694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557314-A-G

2693751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557277-T-C

2693837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557187-G-A

2693837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557187-G-T

2693878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557137-G-A

2693878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557137-G-T

2693979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74557039-T-C

http://identifiers.org/hco/17/GRCh38#2694024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74556994-C-A

2694092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74556929-C-T

http://identifiers.org/hco/17/GRCh38#2694294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74556729-C-A

2694294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556729-C-G

2694597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556485-A-G

2694597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556485-A-T

2694787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556308-T-A

2694787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556308-T-C

2694812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556298-A-G

http://identifiers.org/hco/17/GRCh38#2694842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74556267-C-A

2694842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556267-C-T

http://identifiers.org/hco/17/GRCh38#2694845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74556264-C-A

2694845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556264-C-G

2694845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556264-C-T

http://identifiers.org/hco/17/GRCh38#2695074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74556033-C-A

2695074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74556033-C-T

http://identifiers.org/hco/17/GRCh38#2695273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555838-C-A

2695273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74555838-C-G

2695273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74555838-C-T

http://identifiers.org/hco/17/GRCh38#2695540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555583-C-A

2695540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555583-C-G

2695540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555583-C-T

http://identifiers.org/hco/17/GRCh38#2695641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555447-C-A

2695641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555447-C-T

http://identifiers.org/hco/17/GRCh38#2695709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555356-C-A

2695709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555356-C-T

2695753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555318-G-A

2695807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555281-G-A

2695807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555281-G-T

http://identifiers.org/hco/17/GRCh38#2695836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555241-C-A

2695836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555241-C-G

2695836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555241-C-T

2695837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555240-T-A

2695837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555240-T-C

2695837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555240-T-G

http://identifiers.org/hco/17/GRCh38#2695884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555199-C-A

2695884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555199-C-T

http://identifiers.org/hco/17/GRCh38#2695930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555174-C-A

2695930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555174-C-T

2695948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555156-C-T

2695969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555139-G-A

2695969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555139-G-C

2695969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555139-G-T

http://identifiers.org/hco/17/GRCh38#2695981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74555127-C-A

2695981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555127-C-T

2696040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555066-A-G

2696040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555066-A-T

2696097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74555017-G-T

2696143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74554971-G-A

2696143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74554971-G-C

2696143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74554971-G-T

2696161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 74554953-A-G

http://identifiers.org/hco/17/GRCh38#2696163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74554951-C-A

http://identifiers.org/hco/17/GRCh38#2696194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74554920-C-A

2696194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74554920-C-G

2696194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74554920-C-T

2696208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74554906-A-G

2696209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74554905-G-C

2696209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74554905-G-T

2696211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74554903-T-C

2696308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74554817-T-C

2696692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74554453-T-G

http://identifiers.org/hco/17/GRCh38#2696996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74554111-C-A

http://identifiers.org/hco/17/GRCh38#2697007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74554089-C-A

2697007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74554089-C-T

2697160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74553899-G-A

2697160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74553899-G-C

2697424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74553495-G-A

2697483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74553416-G-A

2697825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74552977-C-G

2698316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74552495-T-C

http://identifiers.org/hco/17/GRCh38#2698556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74552255-C-A

2698757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74552073-G-T

2700178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74551731-C-G

2700829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 74551172-T-A

2700829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 74551172-T-C

http://identifiers.org/hco/17/GRCh38#2700861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74551139-C-A

2700861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74551139-C-T

2700883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74551115-C-G

2700883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74551115-C-T

http://identifiers.org/hco/17/GRCh38#2700951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74551048-A-C

http://identifiers.org/hco/17/GRCh38#2700955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74551045-A-C

2701012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74551006-G-T

2701109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74550932-G-A

2701495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74550543-G-A

2701539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74550499-C-T

2701560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74550482-G-A

2701560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74550482-G-C

2701686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74550358-G-A

2701686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74550358-G-T

2702018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74550049-T-C

http://identifiers.org/hco/17/GRCh38#2702113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74549964-C-A

http://identifiers.org/hco/17/GRCh38#2702203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74549182-C-A

2702261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74549111-C-G

2702270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74549103-A-T

http://identifiers.org/hco/17/GRCh38#2703204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74548275-C-A

2703239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74548246-G-T

2703240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74548245-A-G

2703253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74548235-T-A

2703261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74548213-C-T

http://identifiers.org/hco/17/GRCh38#2703422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74548059-C-A

2703422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74548059-C-T

2703582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74547946-A-G

http://identifiers.org/hco/17/GRCh38#2704228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74547580-C-A

2704228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74547580-C-G

2704447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74547364-G-A

2704447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74547364-G-T

2704504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74547307-G-A

2704504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74547307-G-T

2704528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74547283-G-A

2704528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74547283-G-C

2704528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: missense variant
orthologous variants: 74547283-G-T

2704610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74547204-G-A

http://identifiers.org/hco/17/GRCh38#2704690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74547138-C-A

2704893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74546984-A-G

2705499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74546384-C-G

2705499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74546384-C-T

http://identifiers.org/hco/17/GRCh38#2705840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74545972-C-A

2705968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74545836-T-C

2705970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74545834-G-A

2706133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74545685-G-T

2706135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74545683-A-G

2706141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74545677-G-C

http://identifiers.org/hco/17/GRCh38#2706245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74545601-C-A

2706245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74545601-C-T

2706611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74545289-C-T

2706875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74544894-A-G

http://identifiers.org/hco/17/GRCh38#2706923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74544849-C-A

2706923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74544849-C-G

2706923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74544849-C-T

2707039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74544758-C-T

2707309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74544483-A-G

2707573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74544219-A-G

2707955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74543840-A-G

2708087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74543702-C-T

2708097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74543691-A-G

http://identifiers.org/hco/17/GRCh38#2708107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74543681-C-A

2708162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74543626-C-T

2708179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74543601-G-A

2708231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74543550-C-G

2709052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74542911-T-C

2709680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74542334-C-G

2709754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74542260-G-A

2709796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74542175-C-T

http://identifiers.org/hco/17/GRCh38#2710007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74541970-A-C

2710684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74541381-G-A

2710684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74541381-G-T

2710745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74541315-C-T

2710775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74541285-G-C

http://identifiers.org/hco/17/GRCh38#2710913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74541146-C-A

2710913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74541146-C-T

2711018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74541044-A-G

2711449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540635-A-G

2711468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540616-G-A

2711468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540616-G-C

2711468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540616-G-T

2711471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540613-G-A

2711471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540613-G-C

2711471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540613-G-T

2711599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 74540481-G-A

2711599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 74540481-G-T

2711672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74540411-G-T

http://identifiers.org/hco/17/GRCh38#2711734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74540349-C-A

2711734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74540349-C-T

http://identifiers.org/hco/17/GRCh38#2711778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#74540305-C-A

2711778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 74540305-C-G

2711778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 74540305-C-T

http://identifiers.org/hco/17/GRCh38#2711880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74540204-C-A

2711880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540204-C-T

2711883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540201-G-A

2711883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540201-G-T

2711891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540193-A-G

http://identifiers.org/hco/17/GRCh38#2711924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74540161-C-A

2711924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540161-C-G

2711924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron variant
orthologous variants: 74540161-C-T

2711991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74540094-G-A

2711991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74540094-G-T

2711996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74540089-T-C

http://identifiers.org/hco/17/GRCh38#2712111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74539971-C-A

2712111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74539971-C-T

http://identifiers.org/hco/17/GRCh38#2712120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74539962-C-A

2712305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74539752-G-A

2712305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74539752-G-T

http://identifiers.org/hco/17/GRCh38#2712348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74539705-C-A

2712512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74539550-G-T

http://identifiers.org/hco/17/GRCh38#2712519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74539543-C-A

2712519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29094
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74539543-C-T