56797050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72114714-T-G

56797052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72114712-T-C

56797124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72114640-G-C

56797130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72114634-T-C

56797262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72114290-C-T

56797711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113825-A-G

56797941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113604-A-G

56798181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113366-A-G

56804769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72112870-A-G

56805548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72111737-G-C

56806315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72111586-T-C

56806339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72111558-A-G

http://identifiers.org/hco/15/GRCh38#56806449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72111071-C-A

56811818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72109490-T-A

http://identifiers.org/hco/15/GRCh38#56812547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72108372-C-A

56812547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72108372-C-G

56812682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72108255-T-C

56813206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72107594-G-A

56813418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72107009-T-A

56813418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72107009-T-C

56813612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72106834-T-C

56813668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72106797-G-A

56813731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72106733-G-C

56813817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72106643-C-T

56813845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72106614-C-T

56813850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72106609-A-T

56813993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72106473-C-T

56816818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72105131-T-A

56817014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72104946-C-T

56817054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72104906-T-C

56817358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72104609-A-G

http://identifiers.org/hco/15/GRCh38#56817438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72104531-C-A

56817438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72104531-C-T

56817608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72104373-G-A

56817682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72104300-G-A

56817721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72104261-G-A

56819538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72101904-T-G

56819877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72101478-C-T

56819903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72101457-G-T

56820130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72101264-C-T

56820420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72101039-T-A

56820420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72101039-T-C

56820618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72100924-C-T

56820692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72100855-C-G

http://identifiers.org/hco/15/GRCh38#56820760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72100824-C-A

56820776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72100814-T-C

56821359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72100063-G-A

56821359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72100063-G-T

56821423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72099993-T-A

56821423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72099993-T-C

56821684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72099756-G-A

56821702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72099754-C-T

http://identifiers.org/hco/15/GRCh38#56821921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72099533-C-A

56821921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72099533-C-T

56822255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72099249-A-T

56822436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72099092-G-A

56822627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72098933-T-C

56822736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72098827-T-C

56822855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72098713-C-T

56822896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72098684-C-T

56823078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72098496-G-C

56824002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72097700-G-A

http://identifiers.org/hco/15/GRCh38#56824003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72097699-C-A

56824003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72097699-C-T

56825099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72096902-G-T

56825225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72096774-T-C

56825501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72096211-C-T

56825582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72096118-A-T

56831029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72092702-T-C

56831094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72092639-T-A

56831095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72092638-A-G

56831164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72092554-G-A

56831164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72092554-G-T

56831877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72091980-C-G

56832145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72091721-C-T

56832198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72091664-G-C

56832198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72091664-G-T

56832621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72091173-T-C

56833990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72090436-C-G

56833990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72090436-C-T

56834350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72090083-C-G

56834780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72089683-G-A

http://identifiers.org/hco/15/GRCh38#56834814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72089658-C-A

56835454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72089029-T-C

http://identifiers.org/hco/15/GRCh38#56836402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72087846-A-C

http://identifiers.org/hco/15/GRCh38#56836562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72087704-A-C

56836645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087641-T-A

56836645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087641-T-C

56836842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087460-A-G

56837151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087221-C-T

56837442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086989-G-A

http://identifiers.org/hco/15/GRCh38#56837738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72086496-C-A

56837738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086496-C-G

56838083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086198-A-G

56838439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72085826-A-G

56838831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085340-T-C

56859376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72071862-A-T

56859393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72071834-G-A

56859393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72071834-G-C

56859463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72071772-T-C

http://identifiers.org/hco/15/GRCh38#56859607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72071629-C-A

56859618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72071618-C-G

56859618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72071618-C-T

http://identifiers.org/hco/15/GRCh38#56859619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72071617-A-C

56859619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72071617-A-G

56859716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72071521-T-C

56859717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72071520-C-T

56866159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72068573-T-C

56866159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72068573-T-G

56867870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72067254-G-T

56867947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72067188-A-G

56867996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72067147-G-A

56868224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72066591-T-C

56868392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72066099-G-A

56868392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72066099-G-C

56868512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72065981-G-A

56868523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72065971-G-A

56868652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72065843-T-A

56868856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72065636-G-A

56868856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72065636-G-C

56868856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72065636-G-T

56868937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72065557-A-G

56871158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72063734-G-C

56871158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72063734-G-T

56871234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72063674-T-C

56871317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72063614-C-G

56871390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72063578-A-G

http://identifiers.org/hco/15/GRCh38#56871623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72063360-C-A

56871623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72063360-C-G

56872105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72062921-T-G

56872486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72062511-G-T

56872594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72062410-A-G

56872648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72062349-T-C

56872659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72062336-T-C

56872665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72062330-A-G

56882263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72044813-T-A

http://identifiers.org/hco/15/GRCh38#56882625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72044504-C-A

56883002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72044120-T-C

http://identifiers.org/hco/15/GRCh38#56883070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72044055-C-A

56883493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72043625-A-G

56883661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72043448-C-G

56883762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72043371-G-A

56883898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72043207-A-G

56884957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72042894-C-G

56885022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72042829-C-T

56885080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72042732-G-C

56885080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72042732-G-T

56885716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72042123-C-T

56885864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72041999-A-G

56885987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72041878-C-T

56886088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72041790-A-G

http://identifiers.org/hco/15/GRCh38#56886091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72041787-C-A

56886091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72041787-C-G

56886091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72041787-C-T

56886202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72041577-T-C

http://identifiers.org/hco/15/GRCh38#56886321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72041456-C-A

http://identifiers.org/hco/15/GRCh38#56886475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72041295-C-A

56886475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72041295-C-T

56886767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72041023-A-G

56886940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72040877-C-T

http://identifiers.org/hco/15/GRCh38#56887079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72040763-C-A

56887079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72040763-C-G

56887079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72040763-C-T

56887116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040733-G-A

56887116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040733-G-T

56887127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040722-T-A

http://identifiers.org/hco/15/GRCh38#56887128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72040721-C-A

56887128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72040721-C-T

56887168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 72040705-A-G

56887195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040678-C-T

http://identifiers.org/hco/15/GRCh38#56887238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72040659-C-A

56887238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040659-C-T

56887379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72040514-C-T

56887407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040486-C-G

56887675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040261-T-C

56887678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040258-T-C

56887705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040228-G-T

56887739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040196-G-T

56887750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 72040192-C-T

56887783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040158-G-A

56887783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040158-G-T

http://identifiers.org/hco/15/GRCh38#56887865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72040078-C-A

56887909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72040033-A-T

56887923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72040013-G-A

56887923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72040013-G-T

56887997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72039959-A-G

http://identifiers.org/hco/15/GRCh38#56888013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72039943-C-A

56888013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72039943-C-T

http://identifiers.org/hco/15/GRCh38#56888044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72039914-C-A

http://identifiers.org/hco/15/GRCh38#56888111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72039829-C-A

56888232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72039686-A-G

56888291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72039622-C-T

56888612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72039338-A-G

http://identifiers.org/hco/15/GRCh38#56888910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72038833-C-A

56888910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72038833-C-G

http://identifiers.org/hco/15/GRCh38#56889377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72038270-A-C

56889460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72038189-T-C

56889465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72038184-G-T

56889467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72038182-G-T

56890780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72035323-C-T

56890993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72035117-T-C

56891158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72034951-A-G

56891199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72034911-T-A

56891761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72033999-T-C

http://identifiers.org/hco/15/GRCh38#56891836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72033905-C-A

56891836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72033905-C-G

56891836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72033905-C-T

56892476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72033330-T-A

56893294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72032467-C-T

56893788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72032009-G-C

http://identifiers.org/hco/15/GRCh38#56893802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72031995-A-C

56893855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031955-G-C

56893907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031892-T-C

56894423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031425-G-A

56894914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030974-T-C

56895428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030850-G-T

56895463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030821-G-A

56895620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030672-A-G

56895771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030545-T-C

56895874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030464-A-G

56895874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030464-A-T

56895910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030431-G-A

56896429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030017-T-C

http://identifiers.org/hco/15/GRCh38#56896547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72029930-C-A

56896547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72029930-C-T

56896619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72029855-G-A

56896621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72029853-T-G

56896688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72029777-G-A

56899275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72028501-T-C

56899308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72028470-A-G

56899794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72028069-G-C

56906003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026551-G-A

56907141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026836-C-T

56907350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026626-G-A

56907743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026252-G-C

56907749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026246-C-T

56908034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025256-A-G

http://identifiers.org/hco/15/GRCh38#56908135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72025357-C-A

56908135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025357-C-T

56913634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

56913648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

56913746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022671-T-A

56913746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022671-T-G

56913840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022582-C-T

56913865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022557-A-G

56913890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022540-G-A

56914486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022266-C-T

56914505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022245-C-G

56914505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022245-C-T

56914770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022012-C-G

56915101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021993-T-C

56915209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021881-C-T

56915460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021365-A-G

56915467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021358-G-C

56915597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021166-G-A

56915817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72020970-G-A

56916696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72020277-G-A

56916711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72020262-A-T

56916767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72020206-G-T

56916934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72020110-A-G

http://identifiers.org/hco/15/GRCh38#56916937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72020107-C-A

56916937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72020107-C-T

56917028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72020017-C-T

56917077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non coding transcript exon variant
orthologous variants: 72019993-G-T

56917131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non coding transcript exon variant
orthologous variants: 72019940-A-G

56917512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72019878-A-G

56917711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 72019692-T-C

56917796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non coding transcript exon variant
orthologous variants: 72019626-T-C

http://identifiers.org/hco/15/GRCh38#56918121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72019416-C-A

56918121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 72019416-C-G

http://identifiers.org/hco/15/GRCh38#56918350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72019290-C-A

56918350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 72019290-C-G

56918350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 72019290-C-T

http://identifiers.org/hco/15/GRCh38#56918383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72019281-C-A

56918383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72019281-C-T

http://identifiers.org/hco/15/GRCh38#56918488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72019278-A-C

56918488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72019278-A-G