http://identifiers.org/hco/15/GRCh38#27039533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56954436-C-A

27039533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56954436-C-G

27039593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56954381-C-T

http://identifiers.org/hco/15/GRCh38#27039674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56954322-A-C

27039674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56954322-A-G

27041958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56950448-G-A

27042243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949709-C-G

http://identifiers.org/hco/15/GRCh38#27042465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56949474-C-A

27042474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949467-C-T

27042651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949286-C-G

27042805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949142-G-C

27042818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949128-T-A

27042850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949096-C-G

27042988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948999-C-G

27042988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948999-C-T

27043009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948978-G-A

27043009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948978-G-T

27043105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948891-C-T

27043110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948886-C-G

27043258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948768-G-C

27043294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948734-G-C

27043324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948704-G-A

http://identifiers.org/hco/15/GRCh38#27043350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56948678-C-A

27043393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948635-A-G

27043498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948530-A-G

http://identifiers.org/hco/15/GRCh38#27045478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56948181-C-A

27045478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948181-C-T

27045573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948101-C-T

27045578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948096-A-G

27045655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948018-T-C

http://identifiers.org/hco/15/GRCh38#27045713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56947966-A-C

27045713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947966-A-G

http://identifiers.org/hco/15/GRCh38#27045810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56947899-C-A

27045845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947862-A-T

27046529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947574-T-G

27046621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947500-T-C

http://identifiers.org/hco/15/GRCh38#27046747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56947409-C-A

27046747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947409-C-T

http://identifiers.org/hco/15/GRCh38#27046765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56947391-C-A

27046800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947371-G-A

27046920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947255-C-T

27047014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947160-C-T

27047103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947083-C-G

27047115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947071-C-T

27047161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947029-G-A

27047344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946878-G-T

27047651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946573-C-T

27048102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946104-T-C

27048157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946049-C-T

27048169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946037-C-T

27048175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946031-C-T

27048286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945932-G-T

http://identifiers.org/hco/15/GRCh38#27048322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56945890-A-C

27048322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945890-A-G

http://identifiers.org/hco/15/GRCh38#27048421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56945788-C-A

27048421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945788-C-T

27048533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945693-G-A

27048574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945668-A-G

http://identifiers.org/hco/15/GRCh38#27048614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56945628-A-C

27048897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945181-G-T

27049315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944659-C-T

27049316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944658-G-A

27049527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944489-G-A

http://identifiers.org/hco/15/GRCh38#27049550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56944476-A-C

27049550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944476-A-G

27050728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943153-A-G

27050760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943108-T-C

27050971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56942842-G-A

27056398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938855-A-G

27056445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938814-G-C

27056448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938811-C-T

27056500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938770-C-T

27056656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938636-A-G

27056972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938434-C-T

27057001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938405-C-G

http://identifiers.org/hco/15/GRCh38#27057208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56938033-C-A

27057306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937869-T-C

27057318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937857-G-A

27057318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937857-G-T

27057369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937791-C-G

27057486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937672-T-C

27057494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937670-G-A

27057494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937670-G-T

27057555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937612-G-A

http://identifiers.org/hco/15/GRCh38#27057787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56937225-A-C

27057920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937108-T-C

27058030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937006-C-T

27058059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56936977-C-T

27058104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56936939-T-C

27058897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934992-A-G

27059092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934798-G-T

27059123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934770-C-T

27059299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934606-G-A

27059633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934114-G-T

27059659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934091-T-C

27059912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933818-T-C

27060609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933252-G-T

27060678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933183-T-A

27060697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933165-C-G

27060950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932907-A-G

27061107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932820-C-T

27061436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932534-G-A

27061446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932524-C-G

27061487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932481-C-T

27061518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932451-A-G

http://identifiers.org/hco/15/GRCh38#27061709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56932255-A-C

27061744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932222-C-T

27065693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56931023-G-A

http://identifiers.org/hco/15/GRCh38#27065879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56930856-A-C

27065879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56930856-A-G

27065938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56930791-T-A

27066280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56930481-C-G

27066288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56930477-G-A

27066353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56930419-T-C

27066383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56930389-T-C

27066572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56930203-C-G

27066572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56930203-C-T

http://identifiers.org/hco/15/GRCh38#27066635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56930142-A-C

27066805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56929957-C-G

27070063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56929424-A-T

27070089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56929397-G-A

27070116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56929370-C-T

27070233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56928901-C-T

27070278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56928858-T-C

http://identifiers.org/hco/15/GRCh38#27070738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56924720-A-C

27071133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56924373-G-A

27071259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56924272-T-C

27071457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56924104-G-T

27071475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56924086-A-G

27071540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56924019-A-G

27071900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56923740-G-T

http://identifiers.org/hco/15/GRCh38#27071926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56923714-C-A

27071926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56923714-C-G

27072059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56923538-T-G

http://identifiers.org/hco/15/GRCh38#27072081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56923516-A-C

27072120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56923488-G-A

27072219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56923393-A-G

27072219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56923393-A-T

27074956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56922731-T-C

27074997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56922690-C-T

27075024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56922666-A-G

27075164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56919837-T-C

27077007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918832-C-T

27077102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918743-T-C

27077136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918709-A-G

27077271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918575-G-T

27077272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918574-C-T

27077273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918573-G-A

27077273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918573-G-T

27077427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918335-C-G

http://identifiers.org/hco/15/GRCh38#27077431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56918331-C-A

27077453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918309-C-T

27077698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56918065-G-A

27079661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916721-C-T

http://identifiers.org/hco/15/GRCh38#27079802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56916600-A-C

27079932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916480-A-G

27080024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916381-T-G

27081162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912776-T-A

27081184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912754-C-T

27081220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912726-G-T

27081552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912398-G-A

27081958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912094-T-C

27082288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911846-A-G

27082456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911707-A-T

27082476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911691-A-G

27083084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56910359-A-G

27083198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56910261-G-T

27084073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56908706-G-A

27084073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56908706-G-C

27084083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56908696-G-A

27084182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56908598-T-C

27084270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56908511-T-C

27086885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899770-T-C

27086885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899770-T-G

27087064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899623-C-G

27087064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899623-C-T

27087077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899608-C-T

27087340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56899387-G-A

27087431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899334-G-A

27087585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899186-G-A

27087616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899138-T-A

27087634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899120-A-G

27090867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56899044-G-C

27090935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56898979-T-C

27091120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56898791-C-T

27091204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56898691-G-A

27091483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56898507-A-G

27091483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56898507-A-T

27091694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56898350-A-G

27092164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897985-C-G

27092228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897891-T-C

27092757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897192-A-G

27092830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897119-C-T

http://identifiers.org/hco/15/GRCh38#27095024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56895385-A-C

http://identifiers.org/hco/15/GRCh38#27095102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56895310-A-C

27095905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894023-A-G

27095909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894019-C-G

27095909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894019-C-T

27095950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893980-T-G

27095964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893967-C-T

27095965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893966-G-A

27095965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893966-G-C

27095990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893941-A-G

27096370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893574-T-G

27097569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892051-T-C

27097667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891964-C-T

27097712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891905-G-A

27097712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891905-G-T

27097754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891841-C-G

27097754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891841-C-T

27097763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891833-C-G

27097924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891705-T-G

27097965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891657-T-A

27098009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891594-A-G

27098670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891293-T-C

http://identifiers.org/hco/15/GRCh38#27099236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56890723-C-A

27099270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890689-C-T

27101196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56889440-A-G

27101454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56889169-G-A

27101470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56889153-A-G

27101679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888960-A-G

27102098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888434-G-C

27102124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888409-C-T

27102408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888222-T-A

27102408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888222-T-C

27102408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888222-T-G

27102556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888152-G-A

27102558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56888150-G-T

27103069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887651-G-A

27103192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887530-C-T

27103256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887459-C-T

27103474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887291-C-T

http://identifiers.org/hco/15/GRCh38#27103588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56887184-C-A

27103588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887184-C-T

27103631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887135-C-G

27103645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887121-A-T

27103662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887104-T-C

27103673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887093-G-A

27103865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886948-C-T

27103926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886889-C-T

27103936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886879-T-C

27104007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886810-C-T

27104126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886698-G-A

27121344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859968-C-T

27121405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859907-C-T

27121661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859697-G-A

27122541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859345-C-T

27122622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859270-A-G

27122768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859134-C-G

27123162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858695-T-A

27123429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858492-C-T

27126527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854545-G-A

27126688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854375-T-A

27126760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854307-A-G

27126839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854227-G-A

27126924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854141-C-T

27126959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854105-G-A

27127006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854058-T-C

27134430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852868-C-T

27134595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852703-C-T

27134602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852696-T-A

27134741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852565-T-C

27136118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851751-C-T

27136474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851460-T-G

27136483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851450-G-A

27136583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851273-C-T

27136604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851248-G-A

27136764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851102-A-T

27136900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850948-G-A

http://identifiers.org/hco/15/GRCh38#27136901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56850947-C-A

27136902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850946-C-G

27136982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850863-G-A

27141364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850517-T-A

27141378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850503-G-A

27141512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850395-A-G

27141529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850378-T-C

http://identifiers.org/hco/15/GRCh38#27141572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56850336-C-A

27141577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850331-G-C

27141617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850293-C-T

27141620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850284-T-G

27141624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850280-G-A

27141914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849855-A-G

27143443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849332-G-C

27143443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849332-G-T

27143736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849077-T-A

27143802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849013-T-C

http://identifiers.org/hco/15/GRCh38#27143990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56848859-C-A

27150057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841547-T-C

27150153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841457-T-C

27150243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840957-C-T

27150330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840874-G-A

27150743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840418-C-T

27150815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840365-A-T

27150868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840305-C-T

http://identifiers.org/hco/15/GRCh38#27150953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56840232-C-A

27150964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840221-C-T

27151278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839806-C-G

27151291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839793-T-C

27151687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839440-G-A

27157753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56837007-A-G

http://identifiers.org/hco/15/GRCh38#27157760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56837000-C-A

http://identifiers.org/hco/15/GRCh38#27157890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56836870-C-A

27157957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56836819-G-A

27158064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56836727-G-T

http://identifiers.org/hco/15/GRCh38#27158091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56836702-C-A

27158091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56836702-C-G

27158091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56836702-C-T

27158138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56836653-G-A

http://identifiers.org/hco/15/GRCh38#27158153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56836638-C-A

27158153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56836638-C-T

27158173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836619-T-C

27158387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56836459-G-A

27158387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56836459-G-T

27158432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836418-T-C

27158832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836043-T-C

27158941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56835929-T-C

27159083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40249
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835792-C-T