148697943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47430384-G-A

148698001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47430431-G-A

148698181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430603-A-G

148698324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47430753-G-A

148698324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47430753-G-T

http://identifiers.org/hco/7/GRCh38#148698331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47430760-C-A

148698345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430773-G-A

148698345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430773-G-C

148698345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430773-G-T

148698488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47430911-G-A

148698488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47430911-G-T

148698520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430944-G-A

148698520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430944-G-T

148698559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430980-G-A

148698559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47430980-G-T

148698572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47430992-G-A

148698728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47431128-C-T

148698832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, undefined
orthologous variants: 47431234-G-A

148698832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: intron_variant, undefined
orthologous variants: 47431234-G-T

148699050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47431432-G-A

148699050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47431432-G-T

http://identifiers.org/hco/7/GRCh38#148699126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#47431497-C-A

148699126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47431497-C-T

http://identifiers.org/hco/7/GRCh38#148699150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47431521-C-A

148699150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47431521-C-T

148699266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47431647-C-T

148699577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47431828-G-A

148699816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47432025-C-G

148699816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47432025-C-T

148699994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47432205-G-A

148700653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47432717-C-G

148701335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47433354-C-T

148702443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47434073-A-G

148702937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47434544-A-T

148703596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47435084-G-T

148704265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47435464-A-G

148704726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47436269-G-T

148705518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47437294-G-T

http://identifiers.org/hco/7/GRCh38#148714168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47441980-C-A

148714168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47441980-C-T

148722004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47457203-G-A

148722004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47457203-G-T

148724890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47458663-C-T

148725500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47459148-C-T

148725679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47459267-C-G

148725679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47459267-C-T

148725713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47459292-A-G

148728123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47459826-T-C

148728209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47459899-A-G

148728234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47459921-G-A

148729044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47460782-G-A

148730040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47461756-A-G

148730283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47462000-G-A

148730283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47462000-G-T

148730318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47462035-T-C

148730390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47462106-A-G

148731218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47464199-T-C

148731802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47465927-G-T

148731860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47465958-G-A

148732142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47466248-T-C

148732207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47466341-G-A

148753006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47468554-C-T

http://identifiers.org/hco/7/GRCh38#148753071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47468615-C-A

148753207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47468722-A-T

148753210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47468725-G-T

148753914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47471941-T-A

148753914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47471941-T-C

148753937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47471963-G-A

148753937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47471963-G-T

148754000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 47472025-T-C

http://identifiers.org/hco/7/GRCh38#148754117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47472142-A-C

148754117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47472142-A-G

148754200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47472235-A-G

148754200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47472235-A-T

148755653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47472929-G-T

148755695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47472961-T-C

148755882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47473117-C-T

148755887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47473122-A-G

148756154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47473295-C-T

148756774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47473959-C-G

148756917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47474088-A-G

148757523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47474576-C-T

148758333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47475425-G-T

148758377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47475469-G-T

148759218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47478031-A-T

http://identifiers.org/hco/7/GRCh38#148759451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47478548-C-A

148759451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47478548-C-G

http://identifiers.org/hco/7/GRCh38#148759705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47478759-C-A

148759705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47478759-C-T

148759763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47478814-G-A

148759763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47478814-G-T

148759823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47478851-G-A

148759962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47478991-G-A

148759992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479018-G-A

148760008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479034-T-G

http://identifiers.org/hco/7/GRCh38#148760261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47479291-C-A

148760268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479298-G-A

148760299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479327-G-A

148760299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479327-G-T

148760512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47479540-G-A

http://identifiers.org/hco/7/GRCh38#148760539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47479569-C-A

148760539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47479569-C-T

148760540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47479570-A-G

148760540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47479570-A-T

148760738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47479748-A-T

148762198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47480578-G-A

148762311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47480684-C-T

148762369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47480741-A-T

148763504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47481686-A-G

148764152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482699-G-T

148764515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483100-G-A

148764885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483930-C-T

148765239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484308-C-T

148765878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484793-A-G

148765892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484812-G-C

148766755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485327-T-C

148767058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485478-A-G

148767058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485478-A-T

148767425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485762-A-G

http://identifiers.org/hco/7/GRCh38#148778749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47488309-C-A

148778749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488309-C-T

148778775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488334-G-T

148781696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47489923-A-G

http://identifiers.org/hco/7/GRCh38#148781819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47490027-A-C

148782107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490362-G-A

148782107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490362-G-C

148782153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490407-A-G

148782175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490429-T-C

148782290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490545-A-G

http://identifiers.org/hco/7/GRCh38#148782561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47490649-A-C

148783530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491530-T-C

148783606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491583-A-G

148783688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491663-G-A

148783773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491719-C-T

148784085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 47492028-A-T

148784105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47492048-T-A

148784140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47492080-A-G

http://identifiers.org/hco/7/GRCh38#148786480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47493325-C-A

148786480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493325-C-T

148786506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493364-A-G

http://identifiers.org/hco/7/GRCh38#148786507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47493365-A-C

148786507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493365-A-G

148786686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493522-G-A

148786686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493522-G-T

http://identifiers.org/hco/7/GRCh38#148786915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47493975-C-A

148786915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493975-C-T

148787087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 47494134-C-T

148787654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47494315-C-T

148787705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47494366-T-G

148787926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47494421-A-G

148787979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47494471-A-G

http://identifiers.org/hco/7/GRCh38#148788488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47495021-C-A

148788546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495088-G-A

148788546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495088-G-C

148788873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495383-G-T

148788879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495389-G-A

148789410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495743-G-A

148789458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495788-G-A

148789506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495831-G-A

148789893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496189-G-A

148789893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496189-G-T

148790174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496448-A-G

148790253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496527-G-A

148790253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496527-G-T

148790286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496558-A-G

http://identifiers.org/hco/7/GRCh38#148790654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47496921-A-C

148790654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496921-A-G

148791339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497299-G-C

148791353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497313-A-G

148792792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47497793-C-T

148792883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497887-A-G

148792885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497889-G-A

148792885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497889-G-T

148792892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497893-A-G

148792894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497895-G-A

148798040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500241-A-G

148798041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500242-G-A

148798052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500249-A-G

148798472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500559-A-T

http://identifiers.org/hco/7/GRCh38#148798512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47500593-C-A

148798512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500593-C-G

148798512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500593-C-T

http://identifiers.org/hco/7/GRCh38#148798548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47500609-C-A

148798548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500609-C-T

148798805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500830-A-T

http://identifiers.org/hco/7/GRCh38#148799226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47501406-C-A

148799226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501406-C-T

http://identifiers.org/hco/7/GRCh38#148799247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47501425-A-C

148799247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501425-A-G

148799444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501598-G-A

148799450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501604-A-G

148799481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501632-G-T

148799564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501715-C-T

148799628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501752-G-A

148799628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501752-G-C

http://identifiers.org/hco/7/GRCh38#148799664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47501784-A-C

148799683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501803-T-A

148800174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502196-A-T

148800328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502335-C-T

148800452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502439-G-A

148800452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502439-G-T

http://identifiers.org/hco/7/GRCh38#148800864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47502849-A-C

http://identifiers.org/hco/7/GRCh38#148800877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#47502862-C-A

148800931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47502898-G-A

148800931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2551
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47502898-G-T