57085141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 88755485-G-A

57085141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 88755485-G-C

57085329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88755287-G-T

http://identifiers.org/hco/17/GRCh38#57085791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88754858-C-A

57085791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88754858-C-T

57085945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88754619-G-A

57085945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88754619-G-T

57086037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88754509-G-A

57086037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88754509-G-C

57086037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88754509-G-T

57086065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88754483-G-A

57086068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88754480-T-G

57086138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88754414-G-T

57086141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88754411-G-T

http://identifiers.org/hco/17/GRCh38#57086257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88754293-C-A

http://identifiers.org/hco/17/GRCh38#57086258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88754290-C-A

57086258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88754290-C-T

57086301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88754239-G-A

57086301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88754239-G-T

57086305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88754235-C-G

57086305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88754235-C-T

57086419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88754126-G-T

57086629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88753909-G-A

57086629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88753909-G-T

http://identifiers.org/hco/17/GRCh38#57086655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88753880-A-C

http://identifiers.org/hco/17/GRCh38#57086660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88753875-A-C

57087248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88753267-G-A

57087748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88752558-G-A

57087771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88752536-T-C

57087937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88752398-T-C

57088224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88752146-T-C

57088809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751845-G-A

57088809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751845-G-C

57088809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751845-G-T

57088824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751830-T-C

57088869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751805-A-T

57089537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751414-G-A

57089537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751414-G-C

57089556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751401-A-G

57089818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751139-C-T

57089823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751134-A-G

http://identifiers.org/hco/17/GRCh38#57089831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88751126-C-A

57089831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751126-C-T

57089914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88751039-A-G

57090613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88748847-C-T

57090630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88748820-T-C

57090886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88748610-C-T

57091570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron variant
orthologous variants: 88748034-G-A

57092223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88747565-T-C

57092401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88747395-C-T

57092436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88747348-G-A

57092436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88747348-G-C

57092567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88747232-T-C

57092688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88747114-C-T

57092716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88747093-A-G

http://identifiers.org/hco/17/GRCh38#57092909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88746920-C-A

57092921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746907-G-A

57092921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746907-G-T

57092941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746890-G-A

57092941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746890-G-T

57093165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746678-A-G

http://identifiers.org/hco/17/GRCh38#57093196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88746662-C-A

57093360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746542-C-T

57093361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746541-T-C

57093468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746450-A-G

57093613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746323-G-A

57093613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88746323-G-T

57095503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88743858-T-A

57095503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88743858-T-C

http://identifiers.org/hco/17/GRCh38#57095504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88743857-C-A

57095562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88743752-A-G

57095718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88743580-G-A

57095718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88743580-G-T

57095887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88743434-G-T

57095955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88743269-G-A

57096031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88743083-C-T

57096056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88743060-T-C

57096094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88742965-G-T

57096313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88742604-A-G

57096313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88742604-A-T

57096314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: intron_variant, undefined
orthologous variants: 88742603-G-T

http://identifiers.org/hco/17/GRCh38#57096660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88742266-C-A

57096695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88742230-T-C

57096771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 88742167-T-C

57096912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88742035-T-C

57097236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88741748-C-G

57097236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88741748-C-T

57097634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740908-C-T

57097838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740736-A-G

57097867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740710-C-T

57098078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740501-G-A

57098078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740501-G-C

57098132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740448-G-T

57098315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740265-A-G

57098342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740238-G-A

57098345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740235-G-T

57098532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88740049-T-A

57098540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88740041-G-A

57098556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88740025-G-T

57098575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 88740007-G-A

57098575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 88740007-G-C

57098579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88740003-G-T

57098589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739993-G-A

http://identifiers.org/hco/17/GRCh38#57098617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88739967-A-C

57098617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739967-A-G

57098626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739954-T-C

57098705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739903-G-T

57098710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739898-T-A

57098710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739898-T-C

57098710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739898-T-G

57099611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739338-G-T

57099734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739227-G-T

57099766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739189-T-G

57099862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739085-G-A

57099967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88739011-G-A

57100009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88738981-C-G

57100302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88738677-C-G

http://identifiers.org/hco/17/GRCh38#57105421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88736705-C-A

57105421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88736705-C-T

57105749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88736386-G-A

57105749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88736386-G-T

57105795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88736340-C-T

57105825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88736310-C-T

57105845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88736290-C-G

57105906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88736229-C-T

57106012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, coding_sequence_variant, incomplete_terminal_codon_variant, missense_variant
orthologous variants: 88736130-C-T

57106187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88735969-G-C

57106201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735955-G-A

57106201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735955-G-C

57106246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735910-A-G

57106300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735856-T-A

57106300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735856-T-C

57106307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735849-G-C

57106308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735848-G-A

http://identifiers.org/hco/17/GRCh38#57106324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88735832-C-A

57106324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88735832-C-T

57106337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88735819-A-G

57106551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 88735686-G-T

57106632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88735602-G-A

57106632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88735602-G-C

57106641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88735593-C-T

57106832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 88735429-A-G

57106917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88735344-G-A

57107058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88735203-A-G

http://identifiers.org/hco/17/GRCh38#57107061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88735200-A-C

57107061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88735200-A-G

57107080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88735181-G-A

57107183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88735078-G-T

57107201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88735057-T-G

http://identifiers.org/hco/17/GRCh38#57107213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88735042-C-A

57107213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88735042-C-T

57107230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88735025-G-A

57107230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88735025-G-T

57107266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734986-C-G

57107292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734960-T-G

http://identifiers.org/hco/17/GRCh38#57107309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88734941-C-A

57107309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734941-C-T

http://identifiers.org/hco/17/GRCh38#57107347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88734925-A-C

57107446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88734827-C-T

57107758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734705-A-G

http://identifiers.org/hco/17/GRCh38#57107927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#88734539-C-A

57107927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88734539-C-T

http://identifiers.org/hco/17/GRCh38#57107957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88734509-C-A

57107957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88734509-C-T

57108168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88734311-C-T

57108193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734288-G-A

57108193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734288-G-C

57108193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734288-G-T

57108246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734231-G-A

57108293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88734174-A-G

57108956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88733381-C-G

57108969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88733367-T-C

57108980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88733356-G-T

57108999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88733350-C-T

57109066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88733210-G-A

57109083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88733154-T-C

57109241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88732901-G-A

57109670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88732488-A-G

57109691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88732462-C-G

57109691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88732462-C-T

57109695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88732458-C-T

57109929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88732223-G-T

57110211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731935-G-A

57110211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731935-G-C

57110263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88731905-A-T

57110279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731887-G-A

57110279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731887-G-T

http://identifiers.org/hco/17/GRCh38#57110292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88731882-C-A

57110522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731735-T-G

57110929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731365-G-A

57110929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731365-G-T

http://identifiers.org/hco/17/GRCh38#57111012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88731285-C-A

57111012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731285-C-G

57111012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731285-C-T

57111045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731252-T-G

57111207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731099-G-A

57111296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731033-G-A

57111296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88731033-G-T

57111505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730832-C-T

57111536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88730806-G-A

57111641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730705-A-G

57111659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730687-T-C

57111672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730674-T-G

http://identifiers.org/hco/17/GRCh38#57111682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88730664-C-A

57111682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730664-C-T

57111773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730596-T-C

57111773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730596-T-G

57111934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730439-A-G

57111946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730425-T-C

57111953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730416-T-G

57111978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730398-T-C

57112027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730339-G-T

57112056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730309-G-A

http://identifiers.org/hco/17/GRCh38#57112064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88730301-C-A

57112161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730205-G-T

http://identifiers.org/hco/17/GRCh38#57112352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88730033-A-C

57112352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730033-A-G

57112352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730033-A-T

57112356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730031-G-T

http://identifiers.org/hco/17/GRCh38#57112377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88730006-A-C

57112377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88730006-A-G

http://identifiers.org/hco/17/GRCh38#57112397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88729985-C-A

57112397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729985-C-T

57112409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729973-G-A

57112440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729956-G-A

57112574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 88729798-C-T

57112692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729683-G-A

57112692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729683-G-T

57112791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729600-G-A

57112844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729560-A-G

57112848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729556-G-A

57113468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729060-G-C

57113524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88729006-G-A

57113571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88728961-A-G

57113629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88728865-G-T

57113642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88728835-G-T

57114175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88728233-G-T

http://identifiers.org/hco/17/GRCh38#57114315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88728128-C-A

57114361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88728097-A-T

http://identifiers.org/hco/17/GRCh38#57114393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88728065-C-A

57114393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88728065-C-T

57114465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 88728007-C-T

57114665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727812-G-A

57114665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727812-G-T

57114685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727754-G-A

57114685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727754-G-C

57114707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727732-G-A

57114707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727732-G-T

57114713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727726-G-A

57114713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727726-G-T

57114741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727698-G-A

http://identifiers.org/hco/17/GRCh38#57114758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88727682-C-A

57114758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727682-C-G

57114758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727682-C-T

57114768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727672-G-T

57114769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727671-G-T

57114777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727658-G-A

57114907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727527-T-C

57114926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727372-T-C

57115133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727162-T-C

57115191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727122-T-A

57115191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727122-T-C

57115225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727084-C-T

57115312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88727019-T-C

57115975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726190-T-C

57115998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726169-G-A

57115998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726169-G-T

57116026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726145-C-T

57116037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726134-G-A

57116037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726134-G-T

57116043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726125-T-C

57116062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726105-G-A

57116062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726105-G-C

57116062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726105-G-T

57116087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88726078-C-T

57116153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88726012-G-T

57116320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725862-T-C

57116320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725862-T-G

57116329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725853-G-A

57116352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725827-G-A

57116378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725806-G-A

57116378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725806-G-T

57116393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725793-G-T

57116422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725764-C-T

57116662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725666-T-A

57116692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725639-G-A

http://identifiers.org/hco/17/GRCh38#57116814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88725590-C-A

http://identifiers.org/hco/17/GRCh38#57116909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88725504-A-C

57116960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725463-T-C

http://identifiers.org/hco/17/GRCh38#57116985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88725438-C-A

57116990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725433-T-C

http://identifiers.org/hco/17/GRCh38#57117009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88725420-C-A

57117246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725203-C-T

57117403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725088-T-C

57117411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725080-G-A

57117427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88725064-C-T

57117550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724969-G-A

57117587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724936-C-T

57117640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724862-G-A

57117640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724862-G-T

57117725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724710-C-T

57117751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724683-G-A

57117818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724620-G-A

57117818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724620-G-T

57117830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724605-A-G

http://identifiers.org/hco/17/GRCh38#57118248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88724122-C-A

57118248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724122-C-T

57118267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724103-A-T

57118282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724089-G-A

57118316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724075-G-A

57118316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88724075-G-T

57118474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88723948-G-A

57118474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88723948-G-C

57118474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88723948-G-T

http://identifiers.org/hco/17/GRCh38#57118968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88723212-C-A

57118968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88723212-C-T

57118975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 88723201-T-A

57118982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 88723194-G-A

57119149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88723070-A-G

57119161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88723058-G-A

57119236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88722984-G-A

57119241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88722979-C-T

57120202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88722704-G-T

57120422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722480-T-A

57120422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722480-T-C

57120449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722458-T-A

57120449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722458-T-C

57120449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722458-T-G

57120450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722457-G-A

57120450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722457-G-T

http://identifiers.org/hco/17/GRCh38#57120541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#88722379-C-A

57120541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722379-C-G

57120637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88722317-C-T

57121124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88721852-T-C

57121211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 88721762-T-A

57121319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 367
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 88721647-C-G