77984137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90073634-A-T

77984158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90073657-T-A

77984228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073699-G-A

77984228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073699-G-C

77984228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073699-G-T

http://identifiers.org/hco/15/GRCh38#77984285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90073729-A-C

77984285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073729-A-T

77984349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073758-G-A

77984349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073758-G-C

77984349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073758-G-T

77984359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90073768-T-C

http://identifiers.org/hco/15/GRCh38#77984368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90073777-C-A

77984368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90073777-C-T

77984385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073794-G-A

77984385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073794-G-T

77984438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073853-G-A

77984438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073853-G-T

http://identifiers.org/hco/15/GRCh38#77984461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90073878-A-C

77984461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90073878-A-G

77984461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90073878-A-T

77984581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90073998-G-A

77984581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90073998-G-C

77984581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90073998-G-T

77984634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074049-C-G

77984634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074049-C-T

77984645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074060-T-A

77984645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074060-T-G

http://identifiers.org/hco/15/GRCh38#77984675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074069-C-A

77984675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074069-C-T

http://identifiers.org/hco/15/GRCh38#77984687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074081-C-A

77984687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074081-C-G

77984687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074081-C-T

77984703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074101-G-A

77984703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074101-G-C

77984703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074101-G-T

77984704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074102-A-G

77984704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074102-A-T

77984774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074155-T-C

77984777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074158-C-G

77984913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074263-T-A

77984913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074263-T-C

77984938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074288-T-C

http://identifiers.org/hco/15/GRCh38#77984987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074329-C-A

77984987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074329-C-G

77984987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074329-C-T

77984999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074341-C-G

77984999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074341-C-T

77985003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074345-A-G

77985028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074382-G-A

77985028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074382-G-C

77985028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074382-G-T

77985051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074394-T-C

http://identifiers.org/hco/15/GRCh38#77985060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074403-C-A

77985060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074403-C-T

77985079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074421-T-C

77985126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90074458-G-A

77985126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90074458-G-C

77985126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90074458-G-T

77985352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074685-C-T

77985422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074741-G-A

77985422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074741-G-T

http://identifiers.org/hco/15/GRCh38#77985497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90074818-C-A

77985497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90074818-C-T

77985785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075161-G-A

77985785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075161-G-T

77985831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075207-G-A

77985831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075207-G-T

77985878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075248-G-A

77985878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075248-G-T

77985944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075314-G-A

http://identifiers.org/hco/15/GRCh38#77985968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075338-C-A

77985968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075338-C-T

77986122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075495-G-A

77986122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075495-G-T

http://identifiers.org/hco/15/GRCh38#77986144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075514-C-A

77986144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075514-C-T

77986170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075540-T-C

77986279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075649-C-T

77986375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075742-A-G

77986437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075804-T-A

77986437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075804-T-C

http://identifiers.org/hco/15/GRCh38#77986455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075824-C-A

77986455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075824-C-T

77986466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075835-C-T

http://identifiers.org/hco/15/GRCh38#77986548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90075917-C-A

77986548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075917-C-T

77986569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90075938-T-C

http://identifiers.org/hco/15/GRCh38#77986872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076220-C-A

77986872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90076220-C-T

77986875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90076223-T-C

http://identifiers.org/hco/15/GRCh38#77986916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076264-C-A

http://identifiers.org/hco/15/GRCh38#77987059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90076399-C-A

77987059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076399-C-G

77987059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076399-C-T

77987092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076432-G-A

77987092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076432-G-T

77987100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076440-G-T

77987116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076547-G-A

77987116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076547-G-T

77987166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076634-G-C

77987182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076659-G-C

77987446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076929-G-A

77987518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90076996-C-T

77987692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077108-G-A

77987811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077151-T-A

77987811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077151-T-C

77987811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077151-T-G

http://identifiers.org/hco/15/GRCh38#77987854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077193-C-A

77987854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077193-C-T

77987861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077200-G-A

77987861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077200-G-C

77987861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077200-G-T

77987895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077234-T-A

77987895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077234-T-C

http://identifiers.org/hco/15/GRCh38#77987908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077247-C-A

77987908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077247-C-T

http://identifiers.org/hco/15/GRCh38#77987946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077285-C-A

77987950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077289-G-A

77987950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077289-G-C

77987950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077289-G-T

77987958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077297-G-A

77987958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077297-G-T

77988007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90077346-T-C

77988095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077396-G-A

http://identifiers.org/hco/15/GRCh38#77988098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077399-C-A

77988098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077399-C-T

77988129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077429-G-A

77988129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077429-G-T

77988152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077450-T-A

77988152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077450-T-C

77988152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077450-T-G

77988174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077473-G-C

77988174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077473-G-T

http://identifiers.org/hco/15/GRCh38#77988278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077585-C-A

77988285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077589-T-C

77988354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077625-G-T

http://identifiers.org/hco/15/GRCh38#77988407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077661-C-A

77988407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077661-C-T

77988411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077665-T-A

77988411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077665-T-C

77988561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077828-G-A

77988561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077828-G-T

http://identifiers.org/hco/15/GRCh38#77988566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077833-C-A

77988566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077833-C-G

77988566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077833-C-T

77988576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077843-T-A

77988576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077843-T-C

http://identifiers.org/hco/15/GRCh38#77988582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077849-C-A

77988582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077849-C-G

77988582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077849-C-T

http://identifiers.org/hco/15/GRCh38#77988618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077885-C-A

77988618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90077885-C-T

http://identifiers.org/hco/15/GRCh38#77988653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077920-C-A

77988653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077920-C-G

77988653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077920-C-T

http://identifiers.org/hco/15/GRCh38#77988708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90077975-C-A

77988708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90077975-C-T

http://identifiers.org/hco/15/GRCh38#77988776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078043-C-A

77988776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90078043-C-T

77988891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078162-G-A

77988891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078162-G-T

http://identifiers.org/hco/15/GRCh38#77988896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078170-A-C

77988896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078170-A-G

http://identifiers.org/hco/15/GRCh38#77988908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078182-C-A

77988908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078182-C-T

http://identifiers.org/hco/15/GRCh38#77988953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078223-C-A

77988953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078223-C-T

http://identifiers.org/hco/15/GRCh38#77989221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90078459-A-C

77989221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078459-A-G

77989453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078669-G-A

77989554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078737-G-A

77989554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078737-G-C

77989610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078783-G-A

77989729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078858-T-C

77989750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078869-T-C

77989772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078883-C-T

77989844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078941-T-C

77989945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078976-G-A

77989945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90078976-G-T

http://identifiers.org/hco/15/GRCh38#77989957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079004-C-A

77989957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079004-C-T

77989983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079030-A-G

77989983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079030-A-T

http://identifiers.org/hco/15/GRCh38#77990003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079047-C-A

77990003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90079047-C-T

77990053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079097-G-A

77990053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079097-G-C

77990053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079097-G-T

77990071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079115-A-G

77990160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079204-T-A

77990160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079204-T-C

http://identifiers.org/hco/15/GRCh38#77990161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079205-C-A

77990161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079205-C-T

77990164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079208-G-A

77990164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90079208-G-T

77990190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079222-G-A

77990190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079222-G-T

77990207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079241-A-G

77990214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079248-G-A

77990214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079248-G-T

77990252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079282-T-C

http://identifiers.org/hco/15/GRCh38#77990256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079286-C-A

77990256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079286-C-T

http://identifiers.org/hco/15/GRCh38#77990263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079293-C-A

77990263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079293-C-T

http://identifiers.org/hco/15/GRCh38#77990275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90079302-C-A

77990275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079302-C-G

77990275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079302-C-T

77990311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079334-T-A

77990311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079334-T-C

77990314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079337-A-G

77990753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90079732-G-A

77990800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079764-C-T

77990849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90079815-C-T

77990888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90079854-G-A

77990896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90079862-C-T

77991297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90080179-T-C

77991318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90080200-C-T

77991390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90080268-C-G

http://identifiers.org/hco/15/GRCh38#77991861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90080773-C-A

77991988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90080886-G-A

77992029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90080939-G-C

77992489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90081412-G-A

77992489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90081412-G-T

77992512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90081435-G-A

77992636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90081548-C-T

77992637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90081549-A-G

77992727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90081645-T-A

77992758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90081704-G-C

http://identifiers.org/hco/15/GRCh38#77992980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90081844-C-A

77992980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90081844-C-G

77992980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90081844-C-T

77993028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90081892-T-A

77993028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90081892-T-C

http://identifiers.org/hco/15/GRCh38#77993031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90081895-C-A

77993031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90081895-C-G

77993031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90081895-C-T

http://identifiers.org/hco/15/GRCh38#77993036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90081900-C-A

77993036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90081900-C-T

http://identifiers.org/hco/15/GRCh38#77993151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082021-C-A

77993279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082144-T-A

77993279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082144-T-C

77993279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082144-T-G

77993315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082179-T-C

http://identifiers.org/hco/15/GRCh38#77993349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082209-C-A

77993349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082209-C-G

77993349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082209-C-T

http://identifiers.org/hco/15/GRCh38#77993385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082247-C-A

77993385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082247-C-T

http://identifiers.org/hco/15/GRCh38#77993451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082315-C-A

77993451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082315-C-T

77993485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082349-T-A

77993485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082349-T-C

77993485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082349-T-G

http://identifiers.org/hco/15/GRCh38#77993517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082382-C-A

77993517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082382-C-T

77993565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082428-G-A

77993565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082428-G-T

http://identifiers.org/hco/15/GRCh38#77993588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082466-C-A

77993588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082466-C-T

http://identifiers.org/hco/15/GRCh38#77993602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082475-C-A

77993663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90082538-A-G

http://identifiers.org/hco/15/GRCh38#77993690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082635-C-A

77993690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90082635-C-T

77993727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082746-G-A

77993727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082746-G-T

http://identifiers.org/hco/15/GRCh38#77993765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90082788-C-A

77993765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082788-C-T

77993786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082863-A-G

77993813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082956-T-C

77993814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082957-G-T

77993825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082968-G-A

77993825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90082968-G-T

77993862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083011-T-G

77993863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083012-G-A

77993863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083012-G-T

77993875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90083028-G-A

77993875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90083028-G-C

77993875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90083028-G-T

77993877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90083030-G-A

77993877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90083030-G-T

77993937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90083084-A-G

77994131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083265-A-G

77994160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083290-A-G

77994207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083341-G-A

77994229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083363-G-A

77994435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083591-G-A

77994435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083591-G-C

77994511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083668-A-G

77994512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083677-T-A

77994766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90083919-C-G

http://identifiers.org/hco/15/GRCh38#77994992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90084120-C-A

77995063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 90084181-G-A

77995063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90084181-G-T

http://identifiers.org/hco/15/GRCh38#77995106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90084225-C-A

77995502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90084589-G-A

http://identifiers.org/hco/15/GRCh38#77995531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90084618-C-A

77995697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90084753-G-T

77995734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90084796-G-A

77995734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90084796-G-T

http://identifiers.org/hco/15/GRCh38#77995735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90084797-C-A

77995735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90084797-C-T

77995771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90084848-G-T

77995932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085001-G-A

77996097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085159-G-T

77996109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085173-T-C

http://identifiers.org/hco/15/GRCh38#77996157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90085226-C-A

77996157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085226-C-T

77996237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085349-G-A

77996244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085388-C-T

77996257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085401-G-C

http://identifiers.org/hco/15/GRCh38#77996265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90085409-C-A

77996320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085454-G-T

77996372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085502-C-T

http://identifiers.org/hco/15/GRCh38#77996420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90085541-C-A

77996420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085541-C-T

77996421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085542-T-C

77996469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085608-C-T

http://identifiers.org/hco/15/GRCh38#77996504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90085646-A-C

http://identifiers.org/hco/15/GRCh38#77996516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90085657-C-A

77996555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085688-G-A

77996730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085866-T-G

77996782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085917-A-G

77996836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085969-T-C

77996862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90085990-C-T

77996886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086019-G-C

77996886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086019-G-T

77996891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086024-G-T

77996894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086027-T-C

http://identifiers.org/hco/15/GRCh38#77997104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90086205-C-A

http://identifiers.org/hco/15/GRCh38#77997127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90086230-C-A

77997212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086283-G-A

77997258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086304-T-C

77997332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086352-C-T

http://identifiers.org/hco/15/GRCh38#77997339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90086359-C-A

http://identifiers.org/hco/15/GRCh38#77997558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90086558-A-C

77997749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086704-G-A

77997749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086704-G-T

77997791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086740-G-A

http://identifiers.org/hco/15/GRCh38#77997839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90086783-C-A

77997839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086783-C-G

77997839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086783-C-T

http://identifiers.org/hco/15/GRCh38#77997847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90086791-C-A

77997847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086791-C-T

77998018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086928-T-A

77998018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086928-T-C

77998018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90086928-T-G

http://identifiers.org/hco/15/GRCh38#77998155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90087075-C-A

77998155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90087075-C-T

http://identifiers.org/hco/15/GRCh38#77998156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90087076-C-A

77998156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90087076-C-T

http://identifiers.org/hco/15/GRCh38#77998223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90087143-C-A

77998223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90087143-C-T

http://identifiers.org/hco/15/GRCh38#77998678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90087500-A-C

77998678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087500-A-G

77998816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087604-T-C

77998856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087622-G-A

77998856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087622-G-C

77998856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087622-G-T

77998864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90087629-G-A

77998864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90087629-G-T

77998914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087679-T-G

77998956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087701-T-C

77998956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087701-T-G

77999034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087770-T-C

http://identifiers.org/hco/15/GRCh38#77999038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90087774-C-A

77999038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087774-C-T

77999039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087775-T-C

77999042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087778-G-A

77999042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087778-G-T

77999082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087817-C-T

77999091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087826-G-A

77999094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087829-G-A

77999094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087829-G-C

77999094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90087829-G-T

77999465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088088-T-C

77999516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088134-G-C

77999516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088134-G-T

http://identifiers.org/hco/15/GRCh38#77999523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90088141-C-A

77999527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088144-G-A

77999527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088144-G-T

77999547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088160-G-A

77999782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088345-A-G

77999791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088356-C-T

78000032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90088518-G-A

http://identifiers.org/hco/15/GRCh38#78000261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90088758-A-C

78000540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089011-G-A

78000668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089139-C-T

78000671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089142-C-T

78000797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089275-C-G

78000797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089275-C-T

78000802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089284-C-G

78000825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089307-C-G

78001150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089571-C-G

78001425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089727-T-C

http://identifiers.org/hco/15/GRCh38#78001500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90089776-C-A

http://identifiers.org/hco/15/GRCh38#78001501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90089777-C-A

78001501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089777-C-T

78001526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089800-T-C

78001580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089813-C-T

78001582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089815-T-A

78001582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089815-T-C

78001582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089815-T-G

78001583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089816-G-A

78001583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90089816-G-T

78001738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 90089945-A-G

78001745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90089952-G-A

78001784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90089969-G-T

78001789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90089974-A-G

http://identifiers.org/hco/15/GRCh38#78001961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90090135-C-A

78001982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090141-T-G

78001983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090142-T-A

78001983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090142-T-G

http://identifiers.org/hco/15/GRCh38#78002064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90090235-A-C

78002064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090235-A-G

78002064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090235-A-T

78002065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090236-T-A

78002065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090236-T-C

78002065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90090236-T-G

78002506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90090370-T-G

78002554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90090423-G-T

78003102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90091538-G-A

78003102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90091538-G-T

78003161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90091593-A-G

http://identifiers.org/hco/15/GRCh38#78003206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90091630-C-A

http://identifiers.org/hco/15/GRCh38#78003535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90091951-C-A

http://identifiers.org/hco/15/GRCh38#78003538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90091954-C-A

78003538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90091954-C-T

http://identifiers.org/hco/15/GRCh38#78003588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90092005-C-A

78003588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90092005-C-T

78003590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90092007-A-G

http://identifiers.org/hco/15/GRCh38#78003669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90092095-C-A

78003669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90092095-C-T

http://identifiers.org/hco/15/GRCh38#78003671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90092097-C-A

78003671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90092097-C-G

78003671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90092097-C-T

78003777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90092194-C-T

78003892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90092305-G-A

78003981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90092362-C-T

78004006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90092385-A-G

78004195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90092560-C-G

78004586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90092773-G-A

78004647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90092834-C-T

78004662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90092844-T-C

78004666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90092848-A-G

78005277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90095403-T-G

78006188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90095678-A-G

78006472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90095962-G-C

http://identifiers.org/hco/15/GRCh38#78008023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90096801-C-A

78008024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90096802-T-G

78008078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90096840-G-C

78008297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097046-C-T

78008375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097123-A-G

78008405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097155-G-A

78008579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097261-T-C

78008778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097374-T-C

78008956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097491-T-A

78008956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097491-T-C

78009021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90097555-A-G

78009021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90097555-A-T

http://identifiers.org/hco/15/GRCh38#78009031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90097565-C-A

78009031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90097565-C-T

78009090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90097624-G-C

78009136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097669-G-A

78009136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097669-G-T

http://identifiers.org/hco/15/GRCh38#78009210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90097732-C-A

78009210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097732-C-T

78009220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097742-A-G

78009250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90097772-A-T

78010168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90098088-G-C

78010168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90098088-G-T

http://identifiers.org/hco/15/GRCh38#78010227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90098161-C-A

78010499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90098643-A-G

78010588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90098749-G-C

78010710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90098855-C-T

http://identifiers.org/hco/15/GRCh38#78011146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90099180-A-C

78011399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90099470-C-T

78011435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90099511-C-T

78011494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90099549-A-G

78011494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90099549-A-T

http://identifiers.org/hco/15/GRCh38#78011514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90099569-A-C

78012207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90100034-A-G

http://identifiers.org/hco/15/GRCh38#78012231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90100060-C-A

78012306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90100218-G-T

78012392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90100308-G-A

78012636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90100607-T-A

78012650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90100619-G-T

78012705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90100672-T-A

78012852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90100742-T-C

78012852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90100742-T-G

http://identifiers.org/hco/15/GRCh38#78013024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#90100914-C-A

78013024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90100914-C-G

78013360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90101251-T-C

http://identifiers.org/hco/15/GRCh38#78013445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90101326-C-A

http://identifiers.org/hco/15/GRCh38#78013447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90101328-A-C

78013447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90101328-A-G

78013492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90101409-G-A

78013677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90101658-A-T

78013692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90101667-G-C

78014015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102204-G-A

78014179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102351-G-A

78014272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102430-C-G

78014284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102442-T-C

78014410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102547-C-T

78014552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102653-G-A

78015627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102866-G-A

78015631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102870-T-C

78015730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90102980-C-T

78016016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90103249-G-A

78016063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90103286-T-C

78016348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90104183-C-G

78016412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90104244-G-T

78016457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90104274-T-C

78016515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90104330-C-T

78016653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90104467-T-C

78016731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90104545-G-A

78016731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90104545-G-T

http://identifiers.org/hco/15/GRCh38#78016769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90104584-C-A

78016769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104584-C-T

78016809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104625-T-C

78016810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104626-G-T

http://identifiers.org/hco/15/GRCh38#78016849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90104672-C-A

78016849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104672-C-G

78016849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104672-C-T

78016950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104757-G-A

78016950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104757-G-T

http://identifiers.org/hco/15/GRCh38#78016992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90104781-C-A

78016992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104781-C-T

78017002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104791-G-A

78017002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104791-G-T

http://identifiers.org/hco/15/GRCh38#78017036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90104825-C-A

78017036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104825-C-T

78017039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104828-A-G

78017067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90104856-G-A

http://identifiers.org/hco/15/GRCh38#78017200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90104997-C-A

http://identifiers.org/hco/15/GRCh38#78017220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90105017-C-A

78017220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90105017-C-G

78017220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90105017-C-T

78017338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105121-C-T

78017390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105162-G-A

78017390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105162-G-T

http://identifiers.org/hco/15/GRCh38#78017428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90105211-C-A

78017428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105211-C-G

78017428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105211-C-T

78017564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105258-T-C

http://identifiers.org/hco/15/GRCh38#78017583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90105282-C-A

78017583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105282-C-T

78017706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105368-T-A

78017706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105368-T-G

78017707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105369-G-T

78017740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105391-A-T

http://identifiers.org/hco/15/GRCh38#78017751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90105402-C-A

78017751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105402-C-T

78017757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105408-A-T

78017806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105451-T-C

78017818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105463-G-A

78017818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105463-G-T

http://identifiers.org/hco/15/GRCh38#78017833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90105478-C-A

78017833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105478-C-T

http://identifiers.org/hco/15/GRCh38#78017838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90105483-C-A

78017838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105483-C-T

78017877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90105522-T-C

78017877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90105522-T-G

78017949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90105594-T-A

78017949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90105594-T-C

78017960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90105605-G-A

78017960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90105605-G-C

78017960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90105605-G-T

78017967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105612-A-G

78017991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105640-T-C

78017991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105640-T-G

http://identifiers.org/hco/15/GRCh38#78018080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90105708-C-A

78018097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105726-G-T

78018099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105728-T-A

78018172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105776-G-A

78018293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90105870-T-C

78018438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106013-T-C

78018668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106325-G-C

78018754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106448-A-G

78018768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106475-T-A

78018776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106483-T-A

78018776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106483-T-C

78018824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106530-A-G

http://identifiers.org/hco/15/GRCh38#78018867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90106570-C-A

78018876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90106579-C-T

78023155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107532-C-T

78023306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107643-A-G

78023889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107779-T-C

http://identifiers.org/hco/15/GRCh38#78024072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90107950-C-A

78024072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107950-C-T

78024081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107959-T-A

78024081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107959-T-C

78024085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107963-G-A

78024085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90107963-G-T

78024184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant
orthologous variants: 90108102-C-T

78024192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90108110-A-G

78024249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90108167-C-T

http://identifiers.org/hco/15/GRCh38#78024420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90108338-A-C

78024420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90108338-A-G

78024439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90108357-T-C

78024439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90108357-T-G

http://identifiers.org/hco/15/GRCh38#78024558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90108476-A-C

78024562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90108480-A-G

78024607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90108527-T-C

78024804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90108729-G-A

78025238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90109364-G-A

78025292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90109416-C-G

78025292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90109416-C-T

78025331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90109455-G-A

78025331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90109455-G-C

78025355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90109479-G-A

78025355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90109479-G-C

78025418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90109548-C-T

78029951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90110953-G-A

78029951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90110953-G-T

78029965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90110955-G-A

78029981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90110968-A-G

http://identifiers.org/hco/15/GRCh38#78030026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90111010-C-A

78030026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: synonymous variant
orthologous variants: 90111010-C-G

78030044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: synonymous variant
orthologous variants: 90111028-C-T

http://identifiers.org/hco/15/GRCh38#78030214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90111178-A-C

78030241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90111201-G-A

78030241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90111201-G-C

78030241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90111201-G-T

78033741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90113799-G-A

http://identifiers.org/hco/15/GRCh38#78033812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90113867-A-C

78033864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90114751-T-C

78033939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90114826-T-C

78034284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115109-T-C

78034339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115159-G-T

78034532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90115318-A-G

http://identifiers.org/hco/15/GRCh38#78034558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90115425-C-A

78034587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90115454-T-C

78034587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90115454-T-G

78034634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115497-C-T

78034733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90115574-T-C

http://identifiers.org/hco/15/GRCh38#78034744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90115585-A-C

78034751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115592-A-G

78034782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115622-C-G

78034790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115630-T-A

78035350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115827-C-T

78035513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115990-G-A

78035517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115994-G-A

78035517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90115994-G-C

78035565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116031-G-A

78035565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116031-G-T

78035605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116058-G-A

78035818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116166-C-T

78035990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116326-T-C

78036001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116337-G-C

78036051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116389-A-G

78036087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116409-T-C

78036096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116416-C-G

78036168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116481-G-A

78036214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116527-T-C

78036245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116556-T-G

78036260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116571-C-T

78036279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116590-C-T

78038625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90116946-G-C

http://identifiers.org/hco/15/GRCh38#78038643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90116964-A-C

78038706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117031-T-A

78038706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117031-T-C

78038784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117125-T-C

78039081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117365-T-C

78039134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117419-A-G

78039241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117524-T-C

78039303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117586-G-A

78039361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117644-C-T

78039380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117663-C-T

78039391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117674-C-T

78039447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90117727-G-A

78041003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90118060-A-G

78041052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90118111-G-C

78041208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90118266-T-C

78041362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90118454-G-A

78041958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90119152-G-A

78041958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90119152-G-C

78042091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90119277-A-G

http://identifiers.org/hco/15/GRCh38#78042268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90119428-A-C

78042342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90119578-T-C

78042413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90119650-C-T

78042587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90119794-C-T

http://identifiers.org/hco/15/GRCh38#78042735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90119987-C-A

78043345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90120524-G-A

78044093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122282-G-A

78044102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122291-T-C

78044102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122291-T-G

78044172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122357-T-C

78044427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122599-T-A

78044443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122615-G-A

78044490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122652-G-T

78044607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90122765-T-C

http://identifiers.org/hco/15/GRCh38#78044825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90122978-C-A

http://identifiers.org/hco/15/GRCh38#78044861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90123024-C-A

78044873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90123036-T-A

78044877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90123040-T-A

78044877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90123040-T-C

78044886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90123049-T-C

78044962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 90123125-G-A

http://identifiers.org/hco/15/GRCh38#78045191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90123353-A-C

http://identifiers.org/hco/15/GRCh38#78045322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90123486-C-A

78047296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90124593-C-T

78047316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90124612-T-C

78047331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90124627-C-G

78047331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90124627-C-T

78047657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90124898-C-T

78048068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90125310-G-A

78049072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90126223-T-C

78049205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90126340-G-A

78049232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90126367-C-T

78049797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90126796-C-T

78049977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90126950-C-T

http://identifiers.org/hco/15/GRCh38#78050048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90127021-A-C

78050907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90128095-T-C

78051275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90128433-A-G

78051436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90128584-T-C

78051615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90128752-T-C

78051639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90128784-G-A

78051669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90128809-T-C

http://identifiers.org/hco/15/GRCh38#78051808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90128957-C-A

78052216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90129299-C-T

78052334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90129414-C-G

78053400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90131239-T-C

78053530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90131430-G-C

78053680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90131579-G-A

78053680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90131579-G-C

78053680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90131579-G-T

http://identifiers.org/hco/15/GRCh38#78053705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90131604-C-A

78053943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90131741-T-C

78054081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, missense_variant
orthologous variants: 90131891-G-A

78054270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90132071-G-A

78059280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90135301-A-T

78059294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90135321-G-A

78059342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90135359-A-T

78059347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90135364-T-C

78059562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90135590-C-G

78059588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90135661-C-T

78059619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90135733-A-G

78061924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90137921-G-A

78062821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90139021-C-T

78063371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90139399-A-G

http://identifiers.org/hco/15/GRCh38#78063576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90139588-A-C

78063930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90140044-C-G

78063965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90140080-C-T

http://identifiers.org/hco/15/GRCh38#78064100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90140173-A-C

78064100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90140173-A-G

78064440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90140443-A-T

78064584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90140569-T-C

78065028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141021-C-T

78065124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141114-G-A

78065328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141391-T-C

78065470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141549-C-T

78065535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141613-G-A

78065535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141613-G-C

78066255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141754-A-G

78066268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141766-T-C

http://identifiers.org/hco/15/GRCh38#78066305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90141803-C-A

78066360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90141869-C-T

78066612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90142172-C-T

78066728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90142274-T-A

78066741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90142287-T-A

78066957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90142430-C-T

http://identifiers.org/hco/15/GRCh38#78067019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90142489-C-A

78067229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90142667-T-C

78067278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90142714-T-C

78067583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, undefined
orthologous variants: 90143013-C-T

78067584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, undefined
orthologous variants: 90143014-G-A

78067584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron_variant, undefined
orthologous variants: 90143014-G-C

78067945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90143301-T-C

78068750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90143471-A-T

http://identifiers.org/hco/15/GRCh38#78068764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90143485-A-C

78068833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90143546-G-T

78069138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90143823-C-T

http://identifiers.org/hco/15/GRCh38#78071368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90146684-C-A

78071433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90146753-G-A

78071433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90146753-G-T

78071472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90146797-T-G

78071509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90146834-C-T

78071546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90146873-C-G

78071603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90146930-T-C

78071733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90147059-A-G

78071734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90147060-C-T

78071783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90147106-A-G

78072160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90147805-A-G

78072260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90147885-T-G

78072276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90147901-T-C

78072399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90148029-T-G

78072596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90148237-A-T

http://identifiers.org/hco/15/GRCh38#78072636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90148286-C-A

78072740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90148403-C-T

78073022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90148679-C-T

78073175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90148825-C-G

78073594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90149227-T-C

http://identifiers.org/hco/15/GRCh38#78074663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90150450-C-A

78074663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90150450-C-T

78074881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90150646-T-C

78074989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90150786-A-G

78075022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90150853-T-C

78075040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90150873-C-G

78075161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90150985-G-A

78076012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90151537-G-A

78076012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90151537-G-C

78076012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90151537-G-T

78076115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90151643-A-G

78076213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90151737-T-C

78076791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90151939-T-C

78076901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152032-G-A

78077102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152218-G-A

78077203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152330-G-T

78077222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152354-G-A

78077222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152354-G-C

78077222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152354-G-T

78077233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152365-T-C

78077235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152367-G-A

http://identifiers.org/hco/15/GRCh38#78077236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90152368-C-A

78077236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152368-C-G

78077236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152368-C-T

http://identifiers.org/hco/15/GRCh38#78077261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90152375-C-A

78077261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152375-C-G

78077261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: intron variant
orthologous variants: 90152375-C-T

http://identifiers.org/hco/15/GRCh38#78077347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#90152459-C-A

78077347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 90152459-C-T

78077413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29183
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 90152525-G-A