http://identifiers.org/hco/3/GRCh38#127915241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88604680-C-A

127915241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604680-C-G

127915241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604680-C-T

127915280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604667-G-A

http://identifiers.org/hco/3/GRCh38#127915357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88604612-C-A

127915357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604612-C-T

127915436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604532-G-A

127915436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604532-G-T

127915452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604493-T-C

http://identifiers.org/hco/3/GRCh38#127915462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88604484-C-A

127915478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604468-T-C

127915518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604429-A-G

127915542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604405-G-A

127915626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604341-T-A

127915693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604309-C-T

127915923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88604191-C-T

127916390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88603744-G-A

127919020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88602303-T-C

127919359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88601794-T-C

127919684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88601569-G-A

127919720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88601540-T-C

127919764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88601487-G-T

127920203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88601049-G-C

http://identifiers.org/hco/3/GRCh38#127920238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88601020-C-A

127920250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88601012-T-C

127920411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88600890-G-T

127920643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88600696-T-A

http://identifiers.org/hco/3/GRCh38#127921192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88600129-C-A

127921219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88600102-G-A

127921255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88600064-A-G

127921593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88599695-A-G

http://identifiers.org/hco/3/GRCh38#127922125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88596707-C-A

127922354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88596515-T-C

127922383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88596488-T-C

127922404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88596467-T-G

127922415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88596456-T-C

127922416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88596455-C-T

http://identifiers.org/hco/3/GRCh38#127922995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88595893-C-A

127922995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595893-C-G

127922995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595893-C-T

127923036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595852-T-A

127923036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595852-T-G

127923155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595739-G-T

127923479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595415-G-T

127923542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595352-G-A

127923647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88595247-G-A

127923927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 88594967-C-G

127924073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88594821-G-A

127924752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88594245-A-T

127924876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88594141-C-T

127925527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88593524-A-T

127926008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88592945-A-G

127926011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88592942-A-G

127926346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88592797-A-G

127926932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88592225-G-A

127926988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88592051-G-T

127927353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88591544-T-C

127927885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88591023-A-T

127927894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88591014-C-G

127927894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88591014-C-T

127928107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590815-G-A

127928108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590814-T-C

127928145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590778-A-G

127928192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590730-A-G

127928192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590730-A-T

127928226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590689-T-G

127928254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590661-T-G

127928377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88590537-G-A

127928520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88589895-A-G

127928588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88589831-T-G

127928600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88589819-G-A

127928947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88589538-T-C

127929359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88589193-T-G

http://identifiers.org/hco/3/GRCh38#127929433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88589121-C-A

127929556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88588988-T-C

127929694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88588834-G-A

127929832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88588694-T-C

127929987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88588565-A-G

http://identifiers.org/hco/3/GRCh38#127930022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88588531-C-A

127930022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88588531-C-T

127930029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88588524-C-T

127930334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88588221-A-G

127930951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88587681-G-A

127931041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88587586-G-C

http://identifiers.org/hco/3/GRCh38#127931057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88587579-C-A

127931128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88587511-T-C

127931250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88587397-T-G

127931670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88587138-G-A

127931850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88586979-A-G

127931963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88586132-G-A

127932411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88585747-T-G

127932704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88585458-T-C

127932760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88585431-T-C

127951371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88580330-G-T

127951472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88580234-G-A

127951570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88580141-G-A

127952116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88577385-A-G

127952154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88577348-G-A

127952217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88577068-A-G

127953166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88575351-A-G

127953304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88575250-T-G

127953396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88575169-T-C

127953473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88575095-T-G

127953525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88575043-T-C

127953723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88574819-C-T

127954525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88572469-T-C

127954640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88572350-A-G

127954746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88572269-C-G

127955697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88571533-A-G

127955774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88571475-A-G

127955796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88571454-G-C

127956164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88571123-T-C

127956494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88570878-C-T

127956607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88570620-C-T

127956917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88570335-T-C

127956922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88570330-C-T

http://identifiers.org/hco/3/GRCh38#127957202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88570053-C-A

127957202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88570053-C-T

127957479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88569175-T-G

127957701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88569003-C-T

127957835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88568872-T-C

127957983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88568727-G-A

127958206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88568569-T-A

127958386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88568412-G-A

127958651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88568103-A-G

127958830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88567919-G-C

127959236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88567621-G-A

127959261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88567596-T-C

127959386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88567475-G-A

127959682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88567050-T-C

127959785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566962-G-A

127959787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566960-A-T

http://identifiers.org/hco/3/GRCh38#127959931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88566811-C-A

127959931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566811-C-G

127959931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566811-C-T

127959967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566777-T-C

127959993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566749-G-A

127960123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566631-C-T

127960408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566379-A-T

127960469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88566318-T-C

http://identifiers.org/hco/3/GRCh38#127960784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88565994-A-C

127960784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565994-A-G

127961203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565605-T-G

127961301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565515-A-G

127961333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565490-G-A

127961349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565474-C-T

127961437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565386-T-A

127961437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565386-T-C

127961522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565315-A-G

127961557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88565283-G-A

127961920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564929-A-G

127962076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564806-G-A

127962158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564771-A-G

http://identifiers.org/hco/3/GRCh38#127962299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88564685-C-A

127962299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564685-C-T

127962597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564465-A-G

127962658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564406-G-A

127962814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564241-T-A

127962814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564241-T-G

http://identifiers.org/hco/3/GRCh38#127962993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88564115-A-C

127962994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564114-A-G

127963069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564076-G-C

127963069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564076-G-T

http://identifiers.org/hco/3/GRCh38#127963075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88564070-A-C

127963075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564070-A-G

http://identifiers.org/hco/3/GRCh38#127963076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88564069-A-C

127963077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564068-G-T

http://identifiers.org/hco/3/GRCh38#127963100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88564049-C-A

127963100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88564049-C-T

http://identifiers.org/hco/3/GRCh38#127963199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88563947-C-A

http://identifiers.org/hco/3/GRCh38#127963209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88563937-C-A

127963209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563937-C-G

127963260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563886-C-G

127963260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563886-C-T

127963339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563807-G-C

127963339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563807-G-T

127963341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563805-G-T

127963368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563778-G-A

127963368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563778-G-C

127963368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88563778-G-T

127963716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563562-T-C

127963720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563558-A-G

127963734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563544-A-G

127963767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563511-G-T

127963782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563493-G-T

http://identifiers.org/hco/3/GRCh38#127963926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88563355-C-A

127964024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563267-G-A

127964083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563227-T-C

127964110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563210-G-A

127964163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563159-C-T

127964210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563109-C-G

127964215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88563105-A-G

127980064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88533989-T-C

127980170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88533890-A-G

127980209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88533814-G-T

127984062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88524956-T-G

127984082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88524910-T-G

127984099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 88524893-C-T

127984148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88524844-A-G

127984189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88524803-A-G

127984195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88524797-G-A

http://identifiers.org/hco/3/GRCh38#127984343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88524622-C-A

127984343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524622-C-G

127984343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524622-C-T

http://identifiers.org/hco/3/GRCh38#127984355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88524603-C-A

127984373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524586-T-A

127984373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524586-T-G

127984383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524576-G-C

127984383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524576-G-T

127984392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524567-G-A

127984392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524567-G-C

127984392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524567-G-T

127984408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524551-T-C

http://identifiers.org/hco/3/GRCh38#127984417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88524540-C-A

127984417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524540-C-T

127984422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524535-G-C

127984422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524535-G-T

127984428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524529-G-A

127984428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524529-G-T

127984437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524513-G-A

127984437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524513-G-T

127984446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524504-T-C

127984510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524441-A-G

http://identifiers.org/hco/3/GRCh38#127984518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88524433-C-A

127984518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524433-C-T

127984644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524358-C-T

127984645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524357-A-G

127984645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524357-A-T

127984681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524321-G-T

http://identifiers.org/hco/3/GRCh38#127984731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88524272-A-C

127984732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524271-T-C

127984732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524271-T-G

127984737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524259-T-A

127984737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524259-T-C

http://identifiers.org/hco/3/GRCh38#127984745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88524251-A-C

127984883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524145-T-C

127984946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524106-G-A

127984946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524106-G-T

http://identifiers.org/hco/3/GRCh38#127984951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88524101-C-A

127984951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524101-C-T

127984993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88524064-G-T

http://identifiers.org/hco/3/GRCh38#127985213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523896-C-A

127985213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523896-C-G

127985245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523867-A-G

127985246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523866-G-T

http://identifiers.org/hco/3/GRCh38#127985259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523853-C-A

http://identifiers.org/hco/3/GRCh38#127985303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523804-C-A

127985304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523803-A-G

http://identifiers.org/hco/3/GRCh38#127985317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523793-C-A

127985317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523793-C-G

127985353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523766-A-G

127985454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523674-T-C

127985471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523657-C-T

127985512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523638-G-C

127985512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523638-G-T

127985517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523633-A-G

127985517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523633-A-T

127985518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523632-G-T

http://identifiers.org/hco/3/GRCh38#127985634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523540-C-A

http://identifiers.org/hco/3/GRCh38#127985652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523523-C-A

127985653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523522-T-C

http://identifiers.org/hco/3/GRCh38#127985662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523513-C-A

127985662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523513-C-T

127985699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523491-G-T

127985721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523469-A-G

127985735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523455-T-C

127985750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523440-A-G

127985754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523436-T-C

127985782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523408-G-A

127985915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523290-T-A

127985922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523281-T-C

127985931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523272-A-G

127986021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523200-A-G

http://identifiers.org/hco/3/GRCh38#127986025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88523196-C-A

127986025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523196-C-T

127986326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523004-G-A

127986326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88523004-G-T

127986418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522920-T-A

127986669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522879-A-G

127986840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522828-T-C

127986919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522775-A-G

http://identifiers.org/hco/3/GRCh38#127986938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88522759-C-A

127986999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522726-T-A

127987036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522696-T-C

127987087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522641-G-A

127987087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522641-G-T

127987109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522630-G-A

127987109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522630-G-T

http://identifiers.org/hco/3/GRCh38#127987110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88522629-C-A

127987110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522629-C-T

127987156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522586-A-G

127987193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522567-G-A

127987193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522567-G-T

127987275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522481-A-G

127987291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522466-T-C

127987292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522465-T-C

127987358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522401-G-T

127987379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522380-T-C

http://identifiers.org/hco/3/GRCh38#127987460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88522308-C-A

127987481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_acceptor_variant, undefined
orthologous variants: 88522285-G-T

127987589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25731
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88522175-G-T