89318508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 51805764-T-C

89318535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51805783-G-A

89318535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51805783-G-C

89318535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51805783-G-T

89318538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51805786-G-A

89318538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51805786-G-C

89318538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51805786-G-T

http://identifiers.org/hco/9/GRCh38#89318836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51805950-C-A

89318836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51805950-C-G

89318836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51805950-C-T

89318999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806014-G-A

89318999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806014-G-C

89318999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806014-G-T

89319023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806038-G-A

89319023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806038-G-T

89319029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806044-G-A

89319029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806044-G-C

89319029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806044-G-T

89319197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806170-T-C

89319197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806170-T-G

89319253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51806216-A-G

http://identifiers.org/hco/9/GRCh38#89319288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#51806251-A-C

http://identifiers.org/hco/9/GRCh38#89319469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51806468-C-A

http://identifiers.org/hco/9/GRCh38#89319521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51806520-C-A

89319521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51806520-C-G

89319521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51806520-C-T

89319572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51806561-A-G

89319714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, start_lost, synonymous_variant
orthologous variants: 51806708-A-G

89319720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51806714-A-G

89319724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51806718-T-A

89319792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51806786-G-C

89319845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51806841-T-A

89319852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51806848-G-A

89319852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51806848-G-T

http://identifiers.org/hco/9/GRCh38#89319932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51806935-C-A

89319932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51806935-C-G

89324920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807357-G-A

89324920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807357-G-T

89324936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807373-G-A

89324972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807408-T-C

89324973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807409-A-G

89324998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807430-G-A

89324998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807430-G-T

89325089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807495-G-A

89325159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51807560-G-A

89325287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51808286-G-A

89325287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51808286-G-T

http://identifiers.org/hco/9/GRCh38#89325293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51808292-A-C

89325293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51808292-A-T

89325697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51808693-G-C

89325700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51808697-G-A

89325700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51808697-G-T

89325736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51808728-A-G

89325878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51809111-T-A

89325878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51809111-T-C

89325878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51809111-T-G

89326047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51809285-A-T

89326142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51809361-T-A

89326142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51809361-T-C

89326324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51810445-C-G

89326376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51810506-A-G

89326382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51810512-A-T

89326465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51810582-C-G

http://identifiers.org/hco/9/GRCh38#89328535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51810804-C-A

89328535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51810804-C-T

89328664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51810921-T-G

89328673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51810930-G-A

89328703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51810960-A-G

89328724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51810981-A-G

89328879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51811139-T-C

89328894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 51811154-G-A

89328937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51811197-G-A

89328937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51811197-G-T

http://identifiers.org/hco/9/GRCh38#89328950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51811210-C-A

http://identifiers.org/hco/9/GRCh38#89330455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51812361-C-A

89330492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51812395-A-G

89330492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51812395-A-T

http://identifiers.org/hco/9/GRCh38#89330583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51812481-C-A

89330747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51812646-G-C

89330897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51812749-C-T

89331194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51814303-C-T

http://identifiers.org/hco/9/GRCh38#89331533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51815144-A-C

89332739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51816511-G-A

89332739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51816511-G-T

http://identifiers.org/hco/9/GRCh38#89333050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51816777-C-A

89333050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51816777-C-T

89333091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51816821-A-G

89333374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817125-A-T

http://identifiers.org/hco/9/GRCh38#89333439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51817182-C-A

89333439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817182-C-T

89333440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817183-G-A

89333553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817290-C-T

89333723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817387-A-G

89333840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817487-T-C

89333872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817518-G-C

89333872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817518-G-T

http://identifiers.org/hco/9/GRCh38#89333964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51817573-C-A

89333974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817583-G-T

89334153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 51817754-A-G

89334335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817920-C-G

89334376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817961-C-G

89334376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817961-C-T

http://identifiers.org/hco/9/GRCh38#89334385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51817969-C-A

89334385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51817969-C-G

89334414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51819193-A-G

89334471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51819258-T-C

89334498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51819284-A-G

89334628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 51819414-T-A

89334628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 51819414-T-C

89334628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 51819414-T-G

89334683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51819466-G-T

89335721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51819980-A-G

89335870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51820195-T-C

89335935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51820261-G-A

89338719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825219-G-A

89338719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825219-G-T

89338759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825266-G-T

89338839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825336-T-A

89338848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825345-A-G

89338848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825345-A-T

89338866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825367-C-T

89338869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825370-A-G

89338869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825370-A-T

89338870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825371-G-A

89338886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825389-G-A

89338886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825389-G-C

89338886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825389-G-T

89338910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825404-G-T

89338926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825420-A-G

89338926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825420-A-T

http://identifiers.org/hco/9/GRCh38#89338930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51825424-C-A

89339061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825556-A-G

89339187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825684-G-A

89339260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825725-G-C

89339423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825864-T-C

89339516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51825962-A-T

89339660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51826100-T-G

http://identifiers.org/hco/9/GRCh38#89339721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51826157-C-A

89339721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51826157-C-G

89339721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51826157-C-T

http://identifiers.org/hco/9/GRCh38#89339723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51826159-C-A

http://identifiers.org/hco/9/GRCh38#89339738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51826174-C-A

89339738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51826174-C-T

http://identifiers.org/hco/9/GRCh38#89339999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51827240-C-A

http://identifiers.org/hco/9/GRCh38#89340025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51827266-A-C

89341165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51827747-A-G

89341302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51827874-G-A

89346021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51829461-T-C

89346182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51829630-C-G

89346255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51829793-G-T

89346277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51829815-T-C

89346301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51829839-T-C

89346465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51829991-A-G

89346812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51830288-A-G

http://identifiers.org/hco/9/GRCh38#89347118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51830561-C-A

89347118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51830561-C-G

89347127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51830570-G-A

89348015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831080-G-A

89348015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831080-G-T

http://identifiers.org/hco/9/GRCh38#89348252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51831397-C-A

89348252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831397-C-T

89348403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831522-C-T

89348431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831534-A-G

89348577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831626-G-T

89348606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831659-T-G

89348641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51831696-C-T

89349432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51832574-A-G

89349627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51832750-G-A

89349627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51832750-G-C

89349627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51832750-G-T

89349649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51832777-T-C

89349649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51832777-T-G

http://identifiers.org/hco/9/GRCh38#89349716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51832826-C-A

89349716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51832826-C-T

89349892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51832989-A-G

89349892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51832989-A-T

89349945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51833041-C-T

http://identifiers.org/hco/9/GRCh38#89350034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51833099-C-A

89350034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51833099-C-G

89350034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51833099-C-T

89350093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51833155-C-T

89350662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51833799-G-A

89351092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834163-C-T

89351149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834219-C-T

89351605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834596-C-T

89351631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834622-C-T

89351715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834703-C-T

89351745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834769-G-A

89351841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834852-T-C

89351945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834906-G-A

89351945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51834906-G-T

89356378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51835324-A-G

89356770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835529-G-T

89356872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835627-T-C

89356983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835707-G-A

89356983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835707-G-T

89357011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835736-G-A

89357011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835736-G-T

89357053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835767-A-G

http://identifiers.org/hco/9/GRCh38#89357063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51835777-A-C

89357063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835777-A-G

89357156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835864-G-A

89357156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51835864-G-T

http://identifiers.org/hco/9/GRCh38#89357328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51836000-A-C

89357394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51836015-C-T

89357514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 51836139-T-A

http://identifiers.org/hco/9/GRCh38#89357583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#51836204-A-C

89357650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51836217-G-A

89357684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51836242-G-T

89358093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51836574-C-G

89358479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51837107-T-C

http://identifiers.org/hco/9/GRCh38#89358896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51837485-C-A

89358896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837485-C-G

89358896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837485-C-T

http://identifiers.org/hco/9/GRCh38#89358909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51837499-C-A

89358909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837499-C-T

89358928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51837519-G-A

89359025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837605-G-T

89359062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837642-T-C

89359106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51837688-T-G

89359110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51837692-A-G

http://identifiers.org/hco/9/GRCh38#89359146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#51837720-C-A

89359284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837803-G-A

89359284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837803-G-T

89359494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51837940-A-G

89359766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51838181-G-T

89359874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51838237-A-G

89360284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51838464-T-C

89360385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51838568-A-G

89360725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51838893-G-A

89360725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51838893-G-T

89361134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51839206-G-A

89361134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51839206-G-T

89361138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51839210-G-T

89361188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51839244-G-T

89361316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30972
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51839343-T-C