106930833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131874295-C-T

106930879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131874246-T-C

106931230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131873970-T-C

106931320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131873885-A-G

106931392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131873810-A-G

106931678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131873424-A-G

106932174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131871049-G-A

106932288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870930-C-T

106932291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870927-C-T

106932304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870914-A-G

106932310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870908-C-T

106932353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870863-C-T

106932525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870472-C-T

106932907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870104-A-G

106932994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131870030-G-T

106933055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131869968-G-A

106933105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131869920-T-G

106933392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131869639-C-T

106933732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131869291-T-A

106933811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131869207-G-C

106933988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131869040-A-G

106934154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868954-T-C

106934158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868950-C-G

106934161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868947-G-T

106934319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868800-A-T

106934355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868757-C-G

106934355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868757-C-T

106934422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868713-G-A

106934572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131868593-T-A

106934894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131868109-A-G

106934974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131868029-G-C

106935082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131867933-T-G

106941516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131867622-T-C

106941757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131867382-A-T

106941899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131867235-T-G

106942109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131866999-A-T

106942404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131866667-G-T

http://identifiers.org/hco/4/GRCh38#106942454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131866613-C-A

106942454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131866613-C-G

106942554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131866508-T-A

106942574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131866488-G-A

106942591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131866466-A-G

106943738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131866212-T-C

106944214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131865725-A-T

106944217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131865722-C-T

106944222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131865717-C-T

106944493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131865288-C-T

106944784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131865091-T-A

106945013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131864871-C-T

106945448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131864445-A-T

106945706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131864203-C-G

106945747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131864160-G-A

106946372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131863553-A-T

http://identifiers.org/hco/4/GRCh38#106946405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131863518-A-C

http://identifiers.org/hco/4/GRCh38#106946633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131863307-A-C

106946719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131863223-T-A

106946719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131863223-T-C

106946783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131863165-T-A

106946908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131862770-A-G

http://identifiers.org/hco/4/GRCh38#106947195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131862510-C-A

http://identifiers.org/hco/4/GRCh38#106948045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131862023-C-A

106948045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131862023-C-T

106948119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861957-T-A

106948125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861953-G-A

106948137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861941-T-C

106948202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861874-A-G

106948228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861848-G-C

106948431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861662-T-C

106948478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861617-T-C

http://identifiers.org/hco/4/GRCh38#106948486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131861609-A-C

106948486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861609-A-G

106948529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861534-C-T

106948738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861331-T-C

106949005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861057-T-A

http://identifiers.org/hco/4/GRCh38#106949018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131861044-C-A

106949018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861044-C-G

106949018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131861044-C-T

106949162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860935-G-A

106949191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860908-T-G

106949326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860777-T-A

106949513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860481-A-G

106949539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860455-G-C

106949590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860393-G-A

106949659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860322-C-G

106949687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860296-T-G

106949701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860282-T-C

106949701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860282-T-G

106949784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131860163-T-C

106951684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131859562-C-T

106951820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131859430-T-C

106951922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131859335-T-C

106952940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131859025-C-T

http://identifiers.org/hco/4/GRCh38#106953082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131858892-C-A

106953111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131858864-C-T

106953143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131858832-C-T

http://identifiers.org/hco/4/GRCh38#106953157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131858818-C-A

106953203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131858772-A-G

106953285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131858690-T-C

106953285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131858690-T-G

106953694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131858343-A-T

106954105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131857674-T-G

106954172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131857608-C-T

106954190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131857591-C-T

106954233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131857546-C-T

106954464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131857331-T-A

106954464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131857331-T-G

106955373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131856466-T-C

106955752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131856132-G-C

106955776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131856108-C-T

106955853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131856027-C-G

106955853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131856027-C-T

106958940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131854651-T-C

106959051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131854518-T-A

106959051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131854518-T-C

106959264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131853980-T-A

106959302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131853943-G-A

106959563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131853689-C-T

106959725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131853491-C-T

106959750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131853465-A-G

106960922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131852928-C-T

106961244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131852644-T-C

106961355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131852525-A-T

106962058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131851737-G-A

106962064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131851731-G-T

106962187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131851612-A-G

106965501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131849389-T-C

106966130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131849264-A-G

106966343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131849079-G-C

106966376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131849045-T-C

106966391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131849039-T-C

106966428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131848906-C-G

106966428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131848906-C-T

106966445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131848889-A-T

106967464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131848070-C-T

106967479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131848055-G-A

106967512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131848020-G-T

106967513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131848019-A-G

106967578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847955-A-G

106967676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847850-G-T

106968248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847714-A-G

106968274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847688-A-G

106968317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847643-A-G

106968357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847604-T-C

106968381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847580-T-C

106968534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847471-C-G

106968803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847251-G-A

106968803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847251-G-C

106968871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131847201-A-G

106969204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131846879-A-G

106969224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131846860-G-A

106969359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131846786-T-A

106969561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131846568-T-G

106969628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131846500-C-T

106969705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131846435-G-A

106969705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131846435-G-C

106970062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845808-G-A

http://identifiers.org/hco/4/GRCh38#106970073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131845797-A-C

106970123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845747-A-G

106970131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845739-T-A

106970297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845575-T-G

http://identifiers.org/hco/4/GRCh38#106970595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131845294-A-C

106970595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845294-A-G

http://identifiers.org/hco/4/GRCh38#106970775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131845116-A-C

106970820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845062-G-T

106970821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845061-G-A

106970848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845047-G-A

106970848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131845047-G-C

106971069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131844815-A-G

106971095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131844789-G-A

106971273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131844455-T-C

106971273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131844455-T-G

106971536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131844191-C-G

106971725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131844017-C-G

106971725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131844017-C-T

106971752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131843990-G-A

106971984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131843759-C-G

106972024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131843715-G-T

106972055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131843685-T-C

106979231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131842707-A-T

106979586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131842377-C-T

106981513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131840492-G-T

106981688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131840367-A-G

http://identifiers.org/hco/4/GRCh38#106981733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131840323-A-C

106981844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131840218-T-C

106981886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131840180-T-C

106981984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131840117-A-G

106982224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131839911-A-G

106982309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131839759-G-C

106982450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131839588-G-A

106986005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131838567-T-A

http://identifiers.org/hco/4/GRCh38#106986319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131838248-C-A

106986673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131837911-A-G

106987177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131837391-A-G

106987178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131837390-T-C

106987286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131837307-T-C

106987333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131837265-G-A

http://identifiers.org/hco/4/GRCh38#106987723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131836940-C-A

106987723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131836940-C-T

106988666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131836313-G-A

106989058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835932-A-G

106989137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835842-A-G

106989259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835708-T-C

106989551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835439-A-G

106989772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835052-G-T

106989785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835039-G-A

106989792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835032-T-C

106989792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835032-T-G

106989800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131835024-T-C

106990347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131834432-A-T

106990420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131834357-G-A

106990436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131834344-C-T

106990604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131834227-C-T

106990875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131834055-G-T

106990908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131834022-C-G

106990973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833959-A-G

106990983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833949-G-C

106991020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833916-T-C

106991020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833916-T-G

106991040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833892-A-T

106991155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833773-T-C

106991219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833711-T-C

106991335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833581-C-T

106991388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833529-G-A

106991390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833525-C-T

http://identifiers.org/hco/4/GRCh38#106991627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131833299-C-A

106991708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833213-C-T

106991755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833148-C-T

106991793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833113-C-G

106991793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833113-C-T

106991844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131833071-G-A

106992463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131832631-G-C

http://identifiers.org/hco/4/GRCh38#106992578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131832526-A-C

106992756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131832367-T-C

106992860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131832288-G-A

106992860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131832288-G-T

106992877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131832281-T-C

106992941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131832219-A-G

106993358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831910-G-A

106993665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831630-G-T

106993772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831518-T-C

http://identifiers.org/hco/4/GRCh38#106993840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131831451-A-C

106994019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831274-G-A

106994019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831274-G-C

106994019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831274-G-T

106994145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831147-A-G

106994201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131831093-C-T

106994827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131830070-G-A

106995200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131829626-G-T

106995218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131829607-T-G

106995414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131829420-C-T

106995416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131829414-A-G

106995877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131829095-C-T

106996253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131828856-T-C

106996484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131828636-C-G

106996532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131828589-T-C

106997055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131828238-A-G

106997156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131828138-T-A

106997288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827999-A-G

http://identifiers.org/hco/4/GRCh38#106997368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131827915-C-A

106997368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827915-C-T

106997452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827832-A-G

106998053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827232-G-A

106998061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827224-G-A

106998074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827211-C-T

http://identifiers.org/hco/4/GRCh38#106998075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131827210-C-A

106998075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827210-C-T

106998128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827159-T-C

106998241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131827050-G-T

106998296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131826606-C-T

106998656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131825715-T-C

106998716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131825650-T-C

106999871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131824604-G-A

106999878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131824597-A-G

http://identifiers.org/hco/4/GRCh38#106999881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131824594-C-A

107000185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131824297-A-G

107000298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131824186-T-C

107000428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131824047-A-G

107000489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131823986-G-C

107000508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131823968-T-A

107000508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131823968-T-C

107000519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131823957-A-G

107001029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131823352-T-G

107001382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131823012-G-A

107001470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131822930-T-C

107001599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131822696-T-C

107002957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131821332-T-A

107003010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131821285-A-T

107003026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131821269-T-C

107003061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131821234-G-C

107003068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131821227-G-A

107003289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131821000-T-A

107003387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131820903-T-G

107005863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131820264-C-T

107005976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131820169-A-G

107006682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131818441-C-T

107006784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131818345-T-C

107006794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131818336-A-T

107006848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131818290-T-C

107006895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131818236-T-C

http://identifiers.org/hco/4/GRCh38#107007032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131818121-C-A

107007032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131818121-C-T

107007105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131818052-A-G

107007162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817994-T-G

107007250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817898-G-A

107007278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817870-C-G

107007439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817768-G-A

107007821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817517-T-C

107007835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817486-T-C

107007924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817397-G-A

http://identifiers.org/hco/4/GRCh38#107008089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131817265-C-A

107008117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817243-C-T

107008192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817169-A-T

107008345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131817034-A-G

107008469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131816932-G-A

107008477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131816924-G-A

http://identifiers.org/hco/4/GRCh38#107008539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131816855-C-A

107008539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131816855-C-T

107008582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131816812-A-T

107008722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131816661-T-A

107009007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131815780-C-G

107009072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131815658-T-C

http://identifiers.org/hco/4/GRCh38#107009186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131815547-C-A

107009186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131815547-C-T

http://identifiers.org/hco/4/GRCh38#107009333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131815375-A-C

107009491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131815218-C-T

107009519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131815187-G-A

107009768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131814954-G-A

http://identifiers.org/hco/4/GRCh38#107009846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131814863-A-C

107010386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131814053-C-T

107012548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131813271-T-C

107012561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131813257-G-A

107012624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131813195-G-A

107012904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812915-T-C

107012905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812914-C-T

107013015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812798-C-G

107014926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812564-A-G

107014939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812555-G-A

107015184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812299-T-C

107015355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812130-G-A

107015409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812099-T-G

107015462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131812050-T-C

107015745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131811781-T-G

107016018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131811535-T-C

107016290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131811241-C-T

107016301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131811210-T-C

http://identifiers.org/hco/4/GRCh38#107016475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131811027-C-A

107016790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131810756-G-A

107016790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131810756-G-C

107017096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131810536-T-C

107017202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131810179-T-C

107017212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131810169-C-T

107017234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131810147-A-T

107017520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131809820-T-C

107017721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131809596-C-G

107017947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131809363-G-A

107018228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131809048-T-C

107018491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131808790-T-C

107019472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131807863-G-A

http://identifiers.org/hco/4/GRCh38#107019483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131807850-A-C

107019791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131807546-C-T

107019882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131807471-G-T

107020405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131806962-G-C

107020492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131806876-T-C

107020841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131806727-C-G

107020919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131806652-A-G

107021287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131806275-T-G

http://identifiers.org/hco/4/GRCh38#107021563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131805985-C-A

107021946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805619-C-T

107021976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805593-G-A

107021993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805551-T-A

107021993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805551-T-C

107022237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805342-G-A

107022320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805238-G-A

107022320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805238-G-T

107022418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805143-G-A

107022442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131805119-C-T

107022576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131804980-T-C

107022679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131804811-T-C

107022681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131804809-G-A

http://identifiers.org/hco/4/GRCh38#107022758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131804747-C-A

107022808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131804709-G-T

107022995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131804527-A-G

107023334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131804198-A-T

107024075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131803706-A-T

107024404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131803424-A-G

107025057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802822-C-G

107025057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802822-C-T

107025058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802821-A-G

http://identifiers.org/hco/4/GRCh38#107025102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131802792-C-A

107025102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802792-C-T

107025341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802545-T-G

107025496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802382-G-A

107025543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802335-C-T

107025576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802303-G-C

107025614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131802271-C-T

107026076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131801805-A-G

107026085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131801796-A-G

107026085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131801796-A-T

107026204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131801646-C-T

107026719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131801120-A-T

107026743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131801095-C-G

107027059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800936-C-T

107027321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800688-A-G

107027474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800527-G-A

107027500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800505-A-T

107027522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800481-T-C

107027549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800454-G-T

107027606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800408-G-C

107028336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131800002-G-A

107028400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131799938-T-C

107028411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131799930-T-A

107028411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131799930-T-C

107028760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131799621-T-C

107028882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131799529-G-A

107029064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131799308-A-G

107029723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131798288-T-C

107029956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131797936-T-A

107030525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131797050-A-G

107030697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796890-T-C

107031547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795962-G-T

107031722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795787-C-T

107031898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795601-A-G

107031903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795596-A-G

107031904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795595-T-C

107032104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795356-C-T

107032131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795330-C-G

107032288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795144-G-A

107032638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794758-G-T

107032739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794660-A-G

107033310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794106-A-G

107033368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794046-C-T

107033456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793948-T-C

107033524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793888-C-T

107033537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793875-G-A

107033537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793875-G-T

107033540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793872-T-A

107033540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793872-T-C

107033578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793834-G-A

107033667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793746-G-C

http://identifiers.org/hco/4/GRCh38#107033730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131793700-A-C

107033867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793575-C-G

107033939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793503-G-T

107033959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793449-A-G

107034025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793382-A-G

107034230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131793110-A-G

107034237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131793103-G-A

http://identifiers.org/hco/4/GRCh38#107034440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#131792898-A-C

107034440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131792898-A-T

107034464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131792874-G-C

107034502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792828-A-G

107034555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131792775-G-T

107034627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131792702-A-G

107034803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792547-A-G

107034875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792474-C-T

107035123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792272-G-A

107035123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792272-G-C

107035178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792221-A-G

107035449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131791934-C-G

107035449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131791934-C-T

http://identifiers.org/hco/4/GRCh38#107035558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131791825-A-C

107035582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131791801-A-G

http://identifiers.org/hco/4/GRCh38#107035750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131791625-C-A

107035750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131791625-C-T

http://identifiers.org/hco/4/GRCh38#107035961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131791415-C-A

107035961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791415-C-T

107035965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791411-G-A

107035970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791404-T-A

107035970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791404-T-G

107035996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791378-G-T

http://identifiers.org/hco/4/GRCh38#107036002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131791372-C-A

107036034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791310-T-C

107036034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791310-T-G

107036095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791248-C-T

107036222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791114-C-T

http://identifiers.org/hco/4/GRCh38#107036249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131791087-A-C

107036249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 131791087-A-G

107036477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131790896-C-T

107036614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131790771-G-C

107036865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131790550-G-C

107036955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131790413-T-C

107037005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131790367-C-T

http://identifiers.org/hco/4/GRCh38#107037273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131790055-C-A

107037311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, undefined
orthologous variants: 131790023-T-C

107037626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, undefined
orthologous variants: 131789715-C-G

107037652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, undefined
orthologous variants: 131789687-A-T

http://identifiers.org/hco/4/GRCh38#107037685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131789645-A-C

107037686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131789644-A-G

107038009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131789134-A-T

http://identifiers.org/hco/4/GRCh38#107038147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131789040-A-C

107038188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131788999-G-A

107038721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131788435-G-A

107038805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131788336-T-C

107038890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131788266-C-T

107038978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131788031-C-T

107038979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131788030-T-G

107039216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131787820-A-G

107039406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131787638-T-G

107039432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131787612-C-T

107039629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131787435-T-C

107039630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131787434-A-G

107039634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131787430-T-C

107039817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131787277-A-G

http://identifiers.org/hco/4/GRCh38#107040154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131786978-A-C

107040317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131786804-T-C

107040370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131786751-T-C

107041604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131785349-T-A

107041628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131785330-T-G

107042211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784804-G-A

107042211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784804-G-T

107042250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784776-G-A

107042335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784703-T-G

107042561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784571-C-G

107042694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784452-C-T

107042706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784439-T-C

107042837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131784310-T-C

http://identifiers.org/hco/4/GRCh38#107043609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131783550-A-C

107043820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131783197-T-C

107044194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131782898-C-T

107044216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131782876-T-C

107044311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131782763-T-C

107044563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131782555-T-A

107044617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131782522-A-G

107045158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131782099-T-A

107049852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780952-G-A

107049852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780952-G-T

107050028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780786-T-C

107050141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780682-T-A

107050141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780682-T-C

http://identifiers.org/hco/4/GRCh38#107050347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131780462-A-C

107050415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780393-A-T

107050539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780262-C-G

107050677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780159-C-T

107050779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780052-A-G

107050795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131780032-G-T

http://identifiers.org/hco/4/GRCh38#107050875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131779951-A-C

107050883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131779943-A-G

107052380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131777465-T-C

107053105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131777098-G-A

107053358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131776180-A-G

107053495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131776079-T-C

107053536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131776031-T-C

http://identifiers.org/hco/4/GRCh38#107053551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131776012-C-A

107054087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775763-G-A

107054087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775763-G-T

http://identifiers.org/hco/4/GRCh38#107054139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131775714-A-C

107054139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775714-A-T

107054155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775698-A-G

107054202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775651-T-G

107054233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775621-C-G

107054234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775620-A-T

http://identifiers.org/hco/4/GRCh38#107054863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131775295-C-A

107054863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775295-C-T

107054943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775213-T-C

107054964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131775196-T-C

107055048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131774980-A-G

http://identifiers.org/hco/4/GRCh38#107055306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131774690-C-A

107055362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131774632-A-G

http://identifiers.org/hco/4/GRCh38#107055410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131774582-C-A

107056249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131774065-T-C

107056279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131774040-G-A

107056280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131774039-T-C

107056421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131773910-T-C

107056468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131773864-T-C

107056509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131773825-T-C

107056526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131773808-C-T

107056686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131773667-G-A

107057362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131772682-A-G

107057583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131772471-C-G

107058385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131772053-T-C

107058673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131771791-T-C

107058890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131771601-T-A

107059052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131771441-C-T

107059432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131771072-C-G

107059717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131770781-G-C

http://identifiers.org/hco/4/GRCh38#107059787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131770727-C-A

107060098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131770447-T-C

107060191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131770358-A-G

107060262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131770285-T-A

107060351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131770211-G-A

107060698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131769872-T-G

107060713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131769857-C-T

107061258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131769348-T-G

107062355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131766944-C-T

107062519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131766774-G-T

107062616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131766654-A-G

107062920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131766267-T-G

http://identifiers.org/hco/4/GRCh38#107062921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131766266-C-A

107062946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131766241-T-G

107062979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131766209-A-T

107063334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131765929-G-A

107063689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131765606-T-C

107063885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131765405-G-A

http://identifiers.org/hco/4/GRCh38#107063898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131765393-C-A

107064197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131765124-A-G

107064271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131765051-C-G

107064303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131765025-T-C

107064437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764892-T-A

107064591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764768-T-C

107064934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764452-T-A

107065020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764358-T-C

107065033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764345-G-A

107065033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764345-G-T

107065045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764339-G-C

107065367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131764040-A-G

107066009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131763196-T-C

107066177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131763028-G-A

http://identifiers.org/hco/4/GRCh38#107066226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131762964-C-A

107066226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131762964-C-G

107066601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131762317-C-T

http://identifiers.org/hco/4/GRCh38#107066659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131762269-C-A

107066731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131762203-C-T

107066742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131762193-T-C

107066742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131762193-T-G

107066878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131762061-C-T

107066963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131761977-A-G

107067061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131761901-C-T

107067175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131761784-C-T

107067404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131761364-G-A

107067629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131761137-G-A

107067996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131760793-A-G

107068016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131760772-T-C

107068082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131760696-C-T

107068221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131760558-A-T

107068390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131760390-C-T

http://identifiers.org/hco/4/GRCh38#107068515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131760251-A-C

107068550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131760225-T-C

http://identifiers.org/hco/4/GRCh38#107068569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131760206-C-A

107068674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131760101-T-C

107070823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131759669-C-T

http://identifiers.org/hco/4/GRCh38#107070845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131759647-C-A

107071807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131758731-A-G

107096499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131754367-A-T

107096720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131753261-T-C

107096895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131753096-G-C

107096975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131753014-C-T

107097111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131752881-G-C

107097113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131752879-G-A

107097279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131752637-T-C

http://identifiers.org/hco/4/GRCh38#107097286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131752630-A-C

107105128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131750256-A-T

http://identifiers.org/hco/4/GRCh38#107105516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131749965-C-A

http://identifiers.org/hco/4/GRCh38#107105585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131749911-A-C

107105585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131749911-A-T

107105727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131749766-G-A

107112763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131746247-G-A

107112763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131746247-G-T

107113153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745903-G-A

107113323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745753-A-T

107113349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745724-G-A

107113514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745575-G-A

107113564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745523-G-A

107113770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745337-G-T

107113776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745331-T-A

107113794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745312-C-T

107113943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745173-G-A

107113976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131745143-T-G

107114937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131744017-A-G

107115130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131743858-T-C

107115182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131743805-G-T

107115442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131743541-T-C

107115608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131743378-G-A

107115921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131743214-A-G

107116010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131743137-A-G

http://identifiers.org/hco/4/GRCh38#107117041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131742610-C-A

http://identifiers.org/hco/4/GRCh38#107117393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131742301-C-A

107117393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131742301-C-G

107117394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131742300-T-A

107117532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131741931-T-A

107117751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131741677-T-G

107117825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131741608-C-T

107117965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131741475-C-T

107119172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131740801-G-A

107119271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131740702-C-T

107119351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131740664-C-G

107119351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131740664-C-T

107119535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131740500-G-C

http://identifiers.org/hco/4/GRCh38#107119936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131740156-C-A

107119936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131740156-C-T

107120577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131739510-T-C

107121077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131739025-T-C

107121290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131738825-C-T

107121654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131738474-G-C

107121746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131738378-G-T

http://identifiers.org/hco/4/GRCh38#107121978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131737261-A-C

http://identifiers.org/hco/4/GRCh38#107122032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131737212-A-C

107122132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131737110-A-G

107122142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131737100-T-C

http://identifiers.org/hco/4/GRCh38#107122150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131737092-A-C

http://identifiers.org/hco/4/GRCh38#107122242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131737023-C-A

107122254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131737011-A-G

107124828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131734375-G-C

http://identifiers.org/hco/4/GRCh38#107125074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131733562-C-A

107125234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131733410-T-C

107125420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131733268-T-C

107125480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131733221-A-G

107125486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131733215-A-G

107125543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131733159-T-C

107125661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131733052-T-C

107126199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131731798-C-T

107126278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131731729-G-A

107126278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131731729-G-T

107126435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131731542-G-A

107126488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131731487-T-C

107127264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730865-T-G

107127286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730844-G-T

107127436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730675-A-T

107127536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730610-A-G

107127563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730586-A-G

107127610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730534-T-C

107127829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730334-G-A

107127829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730334-G-T

107128053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730139-G-C

107128114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730078-G-A

107128138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730053-T-A

107128138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131730053-T-C

107128860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131729327-A-G

107129151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131729066-A-G

107129179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131729034-C-G

107129179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131729034-C-T

107129367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131728870-T-C

http://identifiers.org/hco/4/GRCh38#107129374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131728864-C-A

107129743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131728503-C-T

107129794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131728461-C-T

107129998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131728305-T-C

107130366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131727963-C-T

107130477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131727854-T-C

107132323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131724696-C-T

107132399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131724620-A-G

107132732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131724291-T-C

107138588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723852-G-A

107138651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723791-G-A

107138652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723790-G-A

http://identifiers.org/hco/4/GRCh38#107138685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131723759-A-C

107138710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723735-G-A

107138711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723734-T-G

107138756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723713-A-T

107139042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723400-G-A

107139183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131723256-C-G

107139559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131721844-T-C

107139832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131721579-G-A

http://identifiers.org/hco/4/GRCh38#107140058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131721377-C-A

107140233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131721200-T-C

107140333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131721101-A-G

107140456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131720966-G-C

107140485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131720940-T-C

107140897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131720533-A-G

107140977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131720468-C-T

107141170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131720274-C-G

107141251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131720209-A-G

107141251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131720209-A-T

107143894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131718925-G-T

107144212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131718620-T-C

107144534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131717264-G-C

107144564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131717232-T-C

107145070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716464-C-T

107145091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716444-C-T

107145256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716327-T-C

http://identifiers.org/hco/4/GRCh38#107145374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131716225-A-C

107145374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716225-A-G

107145420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716199-G-T

107145425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716194-G-T

107145448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716174-G-A

107145468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131716153-A-G

107145708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131714455-A-G

107145995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131714182-T-G

107146098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131714069-T-C

107146103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131714064-G-A

107146406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131713768-G-C

107146406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131713768-G-T

107146433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131713741-C-G

107146599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131713598-G-A

107146599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131713598-G-T

107147248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131712987-T-C

107147760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131712448-G-A

107147760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131712448-G-C

107147997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131712168-C-T

107148460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131710183-T-C

107148571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131710063-G-A

107148571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131710063-G-T

107148595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131710027-T-A

107148595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131710027-T-G

107148669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131709934-G-A

107148756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131709850-A-G

107148803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131709811-A-G

107149007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131709616-G-T

107149182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131709439-G-A

107149182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131709439-G-T

107149357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131709191-G-C

http://identifiers.org/hco/4/GRCh38#107149741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131708864-A-C

107149889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131708708-T-C

107150045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131708578-T-C

107150112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131708512-T-C

107150114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131708510-C-T

107151049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131707386-T-C

107152052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131707133-G-A

107152080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131707110-G-C

107153112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131706208-T-C

107153175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131706144-G-A

107153417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, undefined
orthologous variants: 131705921-T-C

http://identifiers.org/hco/4/GRCh38#107153462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131705877-C-A

107153632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131705709-T-C

107153637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131705704-C-T

http://identifiers.org/hco/4/GRCh38#107153650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131705691-A-C

107153699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131705654-T-C

107153821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131705534-A-G

http://identifiers.org/hco/4/GRCh38#107154357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131705006-C-A

107154357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131705006-C-T

107154409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131704960-A-G

107154432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131704937-C-T

107154644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131704737-G-A

107154700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131704685-C-G

107155122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131703865-C-T

107155227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131703754-A-G

http://identifiers.org/hco/4/GRCh38#107155448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131703559-C-A

107155479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131703527-A-G

107155638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131703388-C-G

107155638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131703388-C-T

107166535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131697535-A-G

107166665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131697418-A-G

http://identifiers.org/hco/4/GRCh38#107166733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131697140-A-C

107166854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131697017-T-G

107166861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131697010-G-A

107167056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131696833-A-G

107167057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131696832-T-C

107167192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131696697-T-G

107167786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131696100-A-G

107167786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131696100-A-T

107168519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695674-T-G

107168535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695658-T-A

107168535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695658-T-C

107168535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695658-T-G

107168545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695648-T-C

http://identifiers.org/hco/4/GRCh38#107168877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131695308-C-A

107168877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695308-C-T

107168896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695289-A-G

107168969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695234-G-C

http://identifiers.org/hco/4/GRCh38#107169112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131695092-A-C

107169165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131695054-A-G

107169228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131694999-G-A

107169451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131694482-A-T

http://identifiers.org/hco/4/GRCh38#107169590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131694362-A-C

107169664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131694282-G-A

http://identifiers.org/hco/4/GRCh38#107169678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131694268-A-C

http://identifiers.org/hco/4/GRCh38#107169782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131694161-C-A

107169920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131694025-T-G

107169999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131693948-A-G

107169999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131693948-A-T

http://identifiers.org/hco/4/GRCh38#107170001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131693946-A-C

107170001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131693946-A-G

107173377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131691859-G-A

107173603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, undefined
orthologous variants: 131691575-G-C

107173774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131691396-A-T

107173923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131691252-T-A

107173923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131691252-T-C

107173942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131691218-G-A

107174058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131691103-A-G

107174072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131691089-A-G

107174815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131690330-G-T

107175855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131686328-G-A

107175858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131686323-C-T

107175931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131686252-C-G

107175986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131686195-G-A

107175986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131686195-G-T

107176417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685764-A-G

http://identifiers.org/hco/4/GRCh38#107176522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131685664-C-A

107176564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685621-T-C

107176766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685506-C-G

107176835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685441-G-A

107176855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685416-G-A

107176968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685307-T-C

107177000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685268-A-G

107177157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685107-C-T

107177163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685095-T-C

107177174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131685084-T-C

107177577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684694-G-T

http://identifiers.org/hco/4/GRCh38#107177619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131684656-A-C

107177695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684583-T-C

107177695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684583-T-G

107177707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684572-A-T

107177816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684462-T-A

107177823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684454-T-C

107177925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684322-A-G

107177930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131684317-C-T

107178233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131683832-A-G

107178353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131683551-A-G

107178402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131683498-T-C

107178435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131683465-T-C

107178535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131683368-A-G

107178919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131683066-A-G

107179014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131682972-T-A

107179122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131682855-C-G

107179632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131682413-A-T

107183018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131682211-T-C

107183087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131682139-T-G

107183367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131681883-A-G

107183850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131680882-T-C

107184012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131680717-G-A

107184012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131680717-G-T

107188357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131680149-G-A

107188451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5 prime UTR variant
orthologous variants: 131680057-A-G

107188456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5 prime UTR variant
orthologous variants: 131680052-T-C

107188456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5 prime UTR variant
orthologous variants: 131680052-T-G

107188473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5 prime UTR variant
orthologous variants: 131680035-T-C

107188507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5 prime UTR variant
orthologous variants: 131680007-T-C

107188522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5 prime UTR variant
orthologous variants: 131679992-T-C

107188723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131679798-C-T

107188764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131679757-G-A

107189621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131677882-A-G

107189626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131677877-T-C

107189684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131677822-C-T

107190110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131677409-G-T

107190472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131677117-T-A

107191453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131674179-A-G

107192022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131674033-T-A

107192396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131673650-T-C

107192402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131673641-T-A

107192547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131673498-T-A

107193143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131672889-A-T

http://identifiers.org/hco/4/GRCh38#107193237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131672789-A-C

107193531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131672498-A-G

107194056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131671963-T-C

107194157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131671879-C-G

107194157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131671879-C-T

107194721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131671326-T-C

107194773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131671264-G-A

107194802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131671235-T-C

107194805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131671232-A-G

107195411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670654-G-T

107195521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670531-G-A

107195536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670516-A-G

107195639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670415-T-G

107195745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670306-T-C

107195783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670268-C-G

107195783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670268-C-T

107195809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670243-C-T

107195864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670201-G-A

107195864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670201-G-C

107195873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670192-C-T

107195887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670178-G-A

107195887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131670178-G-T

107196067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131669586-T-C

107196124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131669515-C-T

107196171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131669463-G-A

107196288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131669363-T-C

107196494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131669139-C-T

http://identifiers.org/hco/4/GRCh38#107196500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131669133-C-A

107196500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131669133-C-T

107196717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131668925-G-A

107196992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131668654-A-G

107197011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131668635-G-A

107197117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131668533-A-G

107197470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131668222-G-A

107197483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131668106-G-T

107197484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131668105-T-C

107197687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131664216-G-A

107197687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131664216-G-T

107197759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131664131-A-G

http://identifiers.org/hco/4/GRCh38#107197993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131663822-C-A

107197993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131663822-C-T

107198448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131663693-T-C

107198486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131663656-A-G

http://identifiers.org/hco/4/GRCh38#107198633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131663524-C-A

107198790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131663397-T-C

107199076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131662032-T-C

107199285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131661845-G-A

http://identifiers.org/hco/4/GRCh38#107199559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131661584-C-A

107199701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131661461-A-T

107199784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131661375-A-G

107199842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131661320-A-G

107199874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131661288-G-A

107199949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131661061-A-G

107199997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131660998-T-C

107200010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131660983-C-T

107200048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131660955-G-A

107200255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131660754-T-C

107200357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131660641-T-C

107201821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131658987-A-G

107202175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131658548-G-A

107202543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131658205-G-T

http://identifiers.org/hco/4/GRCh38#107204887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131657964-A-C

107204966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657861-C-T

107204967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657860-G-A

107204967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657860-G-C

107205007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657820-C-T

107205030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657801-T-C

107205044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657787-T-C

107205065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657767-C-G

107205065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131657767-C-T

107205239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131650980-T-C

107206084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131649519-C-G

107206140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131649570-G-A

107206263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131649682-G-A

107206264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131649683-T-C

107206341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131649756-G-A

http://identifiers.org/hco/4/GRCh38#107206564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131649931-A-C

107206564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131649931-A-G

107210586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131650046-C-G

107210602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131650059-T-C

107210952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131648957-A-G

107211174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131648727-T-C

http://identifiers.org/hco/4/GRCh38#107211587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131648258-A-C

107211587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131648258-A-G

107211999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131647855-A-G

107212027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131647827-G-A

107212072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131647794-G-T

107212233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131647398-T-A

107212307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131647308-C-T

107212518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131647095-G-C

107212611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131647028-G-C

107212742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131646901-G-C

107212742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131646901-G-T

http://identifiers.org/hco/4/GRCh38#107213029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131646608-A-C

107213193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131646460-T-C

107213892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645783-G-A

107213892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645783-G-C

107213915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645760-A-G

107213997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645675-C-G

http://identifiers.org/hco/4/GRCh38#107214174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131645498-A-C

107214413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645269-C-T

107214428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645254-G-A

107214428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645254-G-C

107214507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645190-T-A

107214615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645084-G-A

107214631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131645068-C-T

107214738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131644966-C-T

107214768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131644926-G-A

107214877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131644825-C-T

http://identifiers.org/hco/4/GRCh38#107216175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131644605-A-C

107216799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643977-T-C

107216941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643841-G-A

107217096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643691-G-A

107217141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643646-G-A

107217150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643637-C-T

107217445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643491-C-T

107217481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643459-T-C

107217821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643112-C-T

107217836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643095-A-G

107217858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643073-T-C

107217885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131643037-T-C

107218064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131642861-C-T

107220807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131640953-G-A

107220811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131640949-A-G

107220822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131640940-C-T

107220924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131640842-T-C

107221149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131634137-T-C

107221267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131634035-T-A

107221308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131633998-T-C

107221684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131633636-T-G

107221955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131633362-T-C

107222460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131632881-A-T

107224319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131632581-T-C

http://identifiers.org/hco/4/GRCh38#107224389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131632493-C-A

107224610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131632279-T-C

107224697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131632217-C-T

107224802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131632110-G-T

107242631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131626351-G-A

http://identifiers.org/hco/4/GRCh38#107242962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131626026-A-C

107243105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625885-G-A

107243105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625885-G-C

107243178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625812-C-G

107243528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625453-G-A

107243560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625417-A-T

107243838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625146-G-A

107243838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625146-G-C

107243911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625084-G-A

107243911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625084-G-T

107243928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131625067-C-T

http://identifiers.org/hco/4/GRCh38#107244004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131624992-A-C

107244014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131624982-T-C

http://identifiers.org/hco/4/GRCh38#107244994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131623809-C-A

107245297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131623557-T-C

107245297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131623557-T-G

107245325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131623529-A-G

107245454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131623426-T-C

107245721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131622924-T-C

http://identifiers.org/hco/4/GRCh38#107245758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131622824-A-C

107245759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131622823-A-T

107245825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131622760-A-G

107245840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131622745-T-C

107246071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131622518-A-G

http://identifiers.org/hco/4/GRCh38#107246081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131622508-A-C

107246319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621907-G-A

107246472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621770-T-G

107246517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621724-C-T

http://identifiers.org/hco/4/GRCh38#107246761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131621322-C-A

107246761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621322-C-T

107246788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621281-T-C

107246893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621176-C-T

107246912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621156-T-G

107247013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131621054-A-T

107247319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131620627-G-C

107247779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131620544-T-C

107247824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131620499-G-A

107247921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131620396-T-C

107248099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131620217-T-C

107248259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131620058-T-C

107248637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131619521-T-G

107248727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131619435-T-C

107250329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131619105-G-A

107250395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131619032-C-G

107250582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618797-A-G

107250628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618724-T-C

107250795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618539-T-G

107250923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618437-T-A

107251043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618319-C-T

107251044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618318-G-A

107251044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618318-G-C

107251096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131618280-A-T

107251505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131617858-G-A

107251525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131617838-T-C

107251534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131617828-T-C

107251556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131617807-G-A

107251671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131617695-T-G

107252315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131616110-A-G

http://identifiers.org/hco/4/GRCh38#107252705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131616514-C-A

107252770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131616579-C-T

107253126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131616922-T-A

107253126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131616922-T-C

107253158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131616961-G-A

107253193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131616996-T-C

107253267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131617072-C-T

http://identifiers.org/hco/4/GRCh38#107253450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131617254-C-A

107253458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131617262-G-A

http://identifiers.org/hco/4/GRCh38#107254064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131615316-A-C

107254109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131615273-C-T

107254290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131615154-T-A

107254378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131615065-T-C

http://identifiers.org/hco/4/GRCh38#107254414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131615029-A-C

107255807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131613302-T-A

107255826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131613283-G-A

107255826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131613283-G-T

http://identifiers.org/hco/4/GRCh38#107255827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131613282-C-A

http://identifiers.org/hco/4/GRCh38#107255862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131613257-A-C

http://identifiers.org/hco/4/GRCh38#107255878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131613241-C-A

107255878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131613241-C-T

107256120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131613030-T-G

107256167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131612943-T-C

107256198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131612908-C-T

107256813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131612462-T-C

107256888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131612386-A-G

107257025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131612308-A-G

107257167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131612144-T-C

107257272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131611878-T-A

107257308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131611842-T-C

107257370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131611813-C-T

107257387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131611796-T-C

107257396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131611779-C-G

107257696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131611143-G-A

107257736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131611104-C-T

107257889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131610998-T-C

107257964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131610990-C-T

107258224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron variant
orthologous variants: 131610687-C-T

107258980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610557-A-G

107258992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610545-A-T

107259001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610535-T-C

107259028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610508-C-T

107259093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610442-T-C

http://identifiers.org/hco/4/GRCh38#107259186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131610375-C-A

107259186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610375-C-T

107259254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610312-T-G

107259257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610309-G-A

http://identifiers.org/hco/4/GRCh38#107259278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131610288-A-C

107259421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131609703-G-A

107259736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131609330-T-C

107259935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131609130-A-G

107260264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131608835-G-A

107260452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131608162-G-A

107260535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131608072-T-A

http://identifiers.org/hco/4/GRCh38#107260586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131608019-C-A

107260764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131607823-T-A

107260879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131607680-T-C

107260882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131607677-G-A

http://identifiers.org/hco/4/GRCh38#107260992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131607574-C-A

http://identifiers.org/hco/4/GRCh38#107261076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131607500-C-A

107261259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131607326-A-T

107261873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131606707-G-A

107261873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131606707-G-C

107262258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131606320-C-T

107262272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131606309-T-C

107262285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131606296-T-C

107262285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131606296-T-G

107266634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599970-G-A

107266634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599970-G-T

107267027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599645-A-G

107267247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599418-A-T

107267253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599412-A-T

107267305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599347-G-A

107267400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599272-T-C

107267428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599247-G-A

107267521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599154-G-A

107267521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599154-G-T

107267642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599038-G-A

107267642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131599038-G-T

107268003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598701-A-G

107268294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598417-T-G

107268345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598367-G-A

107268471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598238-C-T

107268533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598181-A-G

107268533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598181-A-T

107268700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598036-A-G

107268720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131598016-A-T

107274378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131596924-C-T

107274524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131596776-G-A

107274524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131596776-G-C

http://identifiers.org/hco/4/GRCh38#107274564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131596738-A-C

107274603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131596704-C-T

http://identifiers.org/hco/4/GRCh38#107274800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131595820-C-A

107275081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131594184-G-T

107275277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593914-A-G

107275327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593835-G-A

107275364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593793-T-C

107275419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593744-G-A

107275463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593698-G-C

107275504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593666-T-A

107275602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593565-G-A

107275827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131593358-A-T

http://identifiers.org/hco/4/GRCh38#107275848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131593337-C-A

107276464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131592726-G-A

107276545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131592649-G-A

107276577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131592619-G-A

http://identifiers.org/hco/4/GRCh38#107276683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131592001-C-A

http://identifiers.org/hco/4/GRCh38#107276770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131591914-C-A

107276867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131591771-C-T

107276879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131591762-G-A

107276912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131591729-C-T

107277186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131591433-C-T

107277235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131591276-G-A

107277364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131591111-T-C

107277398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131591077-T-C

107277527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131590340-T-C

107277563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131590302-T-C

107277628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131590241-T-C

107277808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131590051-T-A

107277992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131589870-T-C

107278523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131588991-G-A

107278644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131588873-T-G

107278952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131579510-T-C

107279269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131579209-C-T

107279585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131576038-C-G

107279621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131576002-T-C

107279668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575955-C-T

107279691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575932-T-G

107279744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131575894-T-A

107279754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575884-G-A

107279754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575884-G-C

107279754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575884-G-T

107279792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131575846-A-G

107282711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575531-A-G

107282878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575379-C-T

107283063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575197-C-G

107283168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131575076-T-C

107283623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131574722-G-A

107283690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131574659-T-C

107283743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131574607-A-G

107283743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2892
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131574607-A-T