http://identifiers.org/hco/9/GRCh38#120824853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34747996-C-A

120824853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34747996-C-T

120824859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34748001-A-G

120824860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34748002-T-A

120824860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34748002-T-G

120824887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34748040-G-T

120824918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34748074-T-A

120824918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34748074-T-C

120824990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34748189-C-T

http://identifiers.org/hco/9/GRCh38#120825038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34748234-C-A

120825287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34748622-A-T

120826316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34750300-G-A

120826460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34750434-G-A

120826460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34750434-G-T

120826575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34750530-A-G

http://identifiers.org/hco/9/GRCh38#120826696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34750600-C-A

120826782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34750661-G-A

120826782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34750661-G-C

120826988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34750848-T-G

http://identifiers.org/hco/9/GRCh38#120827042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34750900-C-A

120827221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34751063-C-T

http://identifiers.org/hco/9/GRCh38#120827241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34751083-A-C

120827285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34751126-A-G

120827347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34751166-C-T

120827351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34751168-T-A

120827452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34751237-A-G

120827479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34751264-T-G

120827531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34751306-T-C

http://identifiers.org/hco/9/GRCh38#120827982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34752366-C-A

120828471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34752940-T-G

120828668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753009-C-T

http://identifiers.org/hco/9/GRCh38#120828709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34753049-A-C

120828710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753050-G-A

120828730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753089-C-G

120828752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753111-T-C

http://identifiers.org/hco/9/GRCh38#120828986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34753351-C-A

120828986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753351-C-T

120829009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753374-G-A

120829009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753374-G-T

http://identifiers.org/hco/9/GRCh38#120829056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34753422-C-A

120829056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753422-C-T

http://identifiers.org/hco/9/GRCh38#120829094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34753459-C-A

120829120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34753490-G-A

120829120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34753490-G-T

120829218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753588-A-G

http://identifiers.org/hco/9/GRCh38#120829220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34753590-A-C

120829220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753590-A-G

http://identifiers.org/hco/9/GRCh38#120829262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34753618-C-A

120829262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753618-C-G

120829262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34753618-C-T

120829924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34754264-G-A

120830029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34754364-T-C

120830152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34754466-T-A

120830415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34754646-T-C

120830658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34754878-T-C

http://identifiers.org/hco/9/GRCh38#120831186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34755387-C-A

120831186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34755387-C-G

120831186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34755387-C-T

120831193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34755394-G-T

120831275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34755488-A-G

120831318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34755526-C-T

120831325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34755533-T-C

http://identifiers.org/hco/9/GRCh38#120831556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34755761-C-A

120831556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34755761-C-T

120831583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34755806-G-A

120831602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34755822-C-G

120831602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34755822-C-T

120831960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756122-A-G

http://identifiers.org/hco/9/GRCh38#120831962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34756124-C-A

http://identifiers.org/hco/9/GRCh38#120831997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34756155-A-C

120832025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756182-G-A

120832029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756186-A-G

120832029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756186-A-T

120832165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756306-G-A

120832220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756349-A-G

120832241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756370-G-T

120832383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756529-T-C

120832833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756662-C-T

120833083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756874-T-C

120833329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756922-T-C

120833348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756941-G-T

120833399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34756992-C-T

120833435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757028-T-G

120833476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757069-T-A

120833476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757069-T-C

120833485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757074-T-A

120833485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757074-T-C

120833496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757084-C-T

120833537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757118-G-A

120833537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757118-G-C

120833537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757118-G-T

120833540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757121-A-G

http://identifiers.org/hco/9/GRCh38#120833553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34757134-C-A

120833583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757159-A-G

http://identifiers.org/hco/9/GRCh38#120833586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34757162-C-A

120833586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757162-C-T

120834414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757369-G-A

120834678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757691-T-C

120834699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757713-T-G

120834895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34757988-T-C

120834958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34758063-T-G

http://identifiers.org/hco/9/GRCh38#120835020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34758125-C-A

120839418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760039-G-C

120839459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760080-C-G

120839504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760089-A-G

120839512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760097-C-T

120839613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760122-G-A

120839725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760213-T-C

120839746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760234-T-C

http://identifiers.org/hco/9/GRCh38#120842766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34760791-C-A

120842766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760791-C-G

http://identifiers.org/hco/9/GRCh38#120842770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34760795-C-A

120842770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760795-C-T

120842793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760818-C-T

120842829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760854-G-A

120842829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760854-G-C

http://identifiers.org/hco/9/GRCh38#120842892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34760917-C-A

120842892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760917-C-T

120842912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760940-T-A

120842912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34760940-T-C

http://identifiers.org/hco/9/GRCh38#120842958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34760981-C-A

120842983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34761010-T-C

120842983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34761010-T-G

120842986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34761013-C-T

120843016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34761028-G-T

120844087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34761547-G-A

120844313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34761791-G-T

120844323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34761801-C-T

120844450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34761937-A-G

120844491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34761978-T-G

120844675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34762139-T-C

120844738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34762196-G-A

120844797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34762258-C-T

http://identifiers.org/hco/9/GRCh38#120844812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34762274-C-A

http://identifiers.org/hco/9/GRCh38#120845909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34775301-C-A

120845909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775301-C-T

120846643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775443-A-G

120846644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775444-A-G

120846767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775548-G-T

120846785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775566-G-A

120846945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775669-T-C

120846956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775674-G-A

120847143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775764-T-C

120847148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775769-A-G

120847172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34775782-G-A

120847517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776071-G-C

120848822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34777644-G-A

120848827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34777649-G-T

120848846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34777670-C-T

120848861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34777685-C-T

http://identifiers.org/hco/9/GRCh38#120848886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34777709-C-A

120848908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34777731-T-C

http://identifiers.org/hco/9/GRCh38#120848926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34777753-C-A

120849567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778898-G-A

120849567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778898-G-C

120849634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778962-G-A

120849661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778986-G-A

120849756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779074-C-T

120849776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779094-G-A

120849776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779094-G-T

120849852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779130-G-T

120849911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779191-T-C

120850029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779311-G-T

120850301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779422-T-C

120850314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779433-T-C

120850406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34779541-T-C

120850566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34779682-T-C

120850587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34779703-A-G

120850690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779796-G-A

120850690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779796-G-T

120851118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34780181-G-A

120851118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34780181-G-T

http://identifiers.org/hco/9/GRCh38#120851137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34780192-C-A

120851137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34780192-C-T

http://identifiers.org/hco/9/GRCh38#120851148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34780203-A-C

120851148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34780203-A-G

120851149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34780204-G-A

120851149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34780204-G-T

http://identifiers.org/hco/9/GRCh38#120851200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34780256-A-C

120851357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780413-T-G

120851381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780420-G-A

http://identifiers.org/hco/9/GRCh38#120851408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34780447-C-A

120851418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780457-G-T

120851467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780495-C-T

120851486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780514-G-T

120851487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780515-G-T

120851499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780531-T-C

120851505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780537-T-A

120851505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780537-T-C

120851514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780546-C-T

120851578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780603-G-A

120851578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780603-G-T

120851583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780608-C-T

120851911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780881-G-A

120851939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780909-T-C

120851990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780959-G-A

120851990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780959-G-T

120851997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34780966-G-A

http://identifiers.org/hco/9/GRCh38#120852083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34781044-C-A

120852146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781101-A-G

120852196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781151-G-A

120852196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781151-G-T

120852323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781501-A-G

120852489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781709-G-A

120852521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781722-C-T

120852648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781828-C-T

120852652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781832-G-A

120852652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781832-G-T

http://identifiers.org/hco/9/GRCh38#120852663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34781843-C-A

120852663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781843-C-G

http://identifiers.org/hco/9/GRCh38#120852677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34781847-A-C

120852677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781847-A-G

120852680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781850-T-C

http://identifiers.org/hco/9/GRCh38#120852688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34781858-C-A

120852688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781858-C-T

http://identifiers.org/hco/9/GRCh38#120852699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34781869-C-A

120852847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34781958-G-T

120853071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782119-T-C

120853095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782124-A-G

120853096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782125-T-C

120853097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782126-G-A

120853196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782208-A-G

120853255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782226-T-C

120853387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782255-C-T

120853451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782298-G-A

120853490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782327-G-A

120853490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782327-G-T

120853525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782371-T-C

http://identifiers.org/hco/9/GRCh38#120853528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34782374-C-A

120853528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782374-C-T

120853530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782376-A-G

120853530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782376-A-T

http://identifiers.org/hco/9/GRCh38#120853543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34782389-C-A

120853543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782389-C-T

http://identifiers.org/hco/9/GRCh38#120853578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34782394-C-A

120853578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782394-C-T

120853579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782395-A-G

120853582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782398-C-T

120853607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782399-A-T

http://identifiers.org/hco/9/GRCh38#120853618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34782410-C-A

120853618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782410-C-T

120853625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782413-G-A

120853665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782441-G-A

120853665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782441-G-T

http://identifiers.org/hco/9/GRCh38#120853681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34782453-C-A

120853681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782453-C-T

120853733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782507-G-T

http://identifiers.org/hco/9/GRCh38#120853973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34782779-C-A

120854085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34782872-T-C

http://identifiers.org/hco/9/GRCh38#120854150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34783078-C-A

120854190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34783113-G-T

http://identifiers.org/hco/9/GRCh38#120854202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34783123-C-A

120854221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34783140-T-C

120854224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34783143-T-C

120854226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34783145-G-A

120854226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34783145-G-T

http://identifiers.org/hco/9/GRCh38#120854245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34783169-C-A

120854245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27367
most severe consequence: non coding transcript exon variant
orthologous variants: 34783169-C-T