1471781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845548-G-C

1471781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845548-G-T

1471808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845528-G-A

1471808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845528-G-C

1471808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845528-G-T

http://identifiers.org/hco/1/GRCh38#1471818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155845518-C-A

1471818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845518-C-G

1471818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845518-C-T

http://identifiers.org/hco/1/GRCh38#1471823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155845513-C-A

1471823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845513-C-G

1471823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845513-C-T

1471842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845496-G-A

1471842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845496-G-C

1471842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845496-G-T

1471846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845492-G-A

1471846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845492-G-C

1471846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155845492-G-T

http://identifiers.org/hco/1/GRCh38#1471963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155845383-C-A

1471963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense variant
orthologous variants: 155845383-C-G

1471963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense variant
orthologous variants: 155845383-C-T

1471990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense variant
orthologous variants: 155845356-G-A

1471990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense variant
orthologous variants: 155845356-G-T

1472114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, undefined
orthologous variants: 155845234-G-A

1472114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, undefined
orthologous variants: 155845234-G-C

1472179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155845135-T-A

1472179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155845135-T-C

1472179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155845135-T-G

http://identifiers.org/hco/1/GRCh38#1472210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155845099-C-A

1472210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155845099-C-G

1472210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155845099-C-T

1472231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, undefined
orthologous variants: 155845078-G-A

1472231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, undefined
orthologous variants: 155845078-G-C

1472231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, undefined
orthologous variants: 155845078-G-T

1472493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155844870-A-T

1477288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense variant
orthologous variants: 155841609-G-T

1477294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense variant
orthologous variants: 155841603-A-G

1477353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841544-G-A

1477353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841544-G-C

1477353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841544-G-T

1477355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841542-G-A

1477355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841542-G-C

1477371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841534-C-G

1477371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841534-C-T

1477377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841528-G-A

1477377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841528-G-C

1477378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841527-G-A

1477383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841522-G-A

1477383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841522-G-C

1477399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841513-A-G

1477404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841508-T-C

1477434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841482-A-G

1477444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841472-G-A

1477444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841472-G-T

1477531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841417-G-A

1477548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841400-G-A

1477553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841395-G-A

1477740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841227-C-T

1477777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841192-C-T

1477823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron variant
orthologous variants: 155841162-A-G

1477863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155841119-G-A

1477863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155841119-G-T

1477902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155841101-C-T

1477982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155841029-G-A

1477982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155841029-G-T

1477984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155841027-A-G

1478008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155840997-T-G

http://identifiers.org/hco/1/GRCh38#1478530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155840717-A-C

1478530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155840717-A-G

1478530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155840717-A-T

1478535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155840712-A-G

1478580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155840667-G-A

1478589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155840658-G-A

1478589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155840658-G-T

1478592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155840656-A-T

1478594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155840654-G-A

1478594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155840654-G-T

http://identifiers.org/hco/1/GRCh38#1478762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155840497-C-A

1478763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840496-C-G

1478763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840496-C-T

1478968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840301-G-A

http://identifiers.org/hco/1/GRCh38#1479070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155840172-C-A

1479070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155840172-C-G

1479126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840115-T-G

1479129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840112-G-A

1479129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840112-G-C

1479129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840112-G-T

1479159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840079-G-A

1479159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840079-G-T

1479176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155840069-A-T

1479348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839917-C-T

1479350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839915-C-G

http://identifiers.org/hco/1/GRCh38#1479378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155839896-A-C

1480436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839695-G-A

1480454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839681-G-T

1480466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839666-C-T

1480501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839631-C-G

1480538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839596-T-C

1480538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839596-T-G

1480562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839574-C-T

http://identifiers.org/hco/1/GRCh38#1480610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155839535-C-A

1480610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839535-C-T

1480695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839463-G-A

1480701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839457-C-T

1480772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839374-G-A

1480772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839374-G-C

1480772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839374-G-T

1480816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839329-G-T

1480823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839322-T-G

1480827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839318-G-A

1480827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839318-G-T

1480831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839314-T-C

http://identifiers.org/hco/1/GRCh38#1480876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155839272-A-C

1480876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155839272-A-G

1480897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 155839251-C-T

1480909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 155839239-G-A

1480909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 155839239-G-C

1480945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839203-T-C

1480945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155839203-T-G

1481995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838634-G-A

1481995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838634-G-T

1482056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838581-T-C

1482076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838564-T-C

1482106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838539-T-A

1482110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838535-G-A

1482149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155838491-C-G

1482149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155838491-C-T

1482200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155838440-G-T

1482236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155838404-G-A

http://identifiers.org/hco/1/GRCh38#1482275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155838365-C-A

1482275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155838365-C-T

1482299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155838341-A-G

http://identifiers.org/hco/1/GRCh38#1482315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155838325-C-A

1482315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838325-C-T

http://identifiers.org/hco/1/GRCh38#1482316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155838324-C-A

1482316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838324-C-G

1482316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155838324-C-T

1482559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155838077-T-G

1482676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155837948-G-A

1482676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155837948-G-T

1484200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836855-G-T

http://identifiers.org/hco/1/GRCh38#1484256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836798-C-A

1484256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836798-C-T

1484303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836746-C-G

1484327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836723-T-C

http://identifiers.org/hco/1/GRCh38#1484346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836704-A-C

1484346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836704-A-G

http://identifiers.org/hco/1/GRCh38#1484383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836668-C-A

1484383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836668-C-G

1484383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836668-C-T

1484392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836662-A-G

1484400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836654-T-C

http://identifiers.org/hco/1/GRCh38#1484422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836630-C-A

1484422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836630-C-T

1484459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836581-G-A

1484459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836581-G-C

1484459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836581-G-T

http://identifiers.org/hco/1/GRCh38#1484499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836544-C-A

1484499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836544-C-T

1484510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836530-T-C

1484511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836529-A-T

1484517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836523-G-A

1484517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836523-G-T

1484529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836514-G-T

1484539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836504-G-A

1484539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836504-G-C

1484539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836504-G-T

1484566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836485-A-G

http://identifiers.org/hco/1/GRCh38#1484633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836417-C-A

1484633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836417-C-T

http://identifiers.org/hco/1/GRCh38#1484679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836372-C-A

1484679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836372-C-G

http://identifiers.org/hco/1/GRCh38#1484717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836315-C-A

1484717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836315-C-T

http://identifiers.org/hco/1/GRCh38#1484747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836296-C-A

1484747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836296-C-T

1484752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836291-T-C

http://identifiers.org/hco/1/GRCh38#1484791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836253-C-A

1484791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836253-C-G

1484791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836253-C-T

1484809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836229-G-A

1484809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836229-G-T

1484811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836227-G-T

http://identifiers.org/hco/1/GRCh38#1484836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836198-C-A

1484836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836198-C-T

1484845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836189-A-T

http://identifiers.org/hco/1/GRCh38#1484847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836187-C-A

1484847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836187-C-T

1484865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836166-G-A

1484865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836166-G-C

1484865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836166-G-T

1484867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836164-G-T

http://identifiers.org/hco/1/GRCh38#1484878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155836153-C-A

1484878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836153-C-T

1484893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836144-C-T

1484902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836135-G-A

1484902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836135-G-C

1484902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836135-G-T

1484926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836112-G-T

1484949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836089-T-C

1484979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836073-T-G

1485007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836056-C-G

1485007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155836056-C-T

1485179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155835884-C-T

1485193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835873-T-G

1485200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835866-G-A

1485200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835866-G-C

http://identifiers.org/hco/1/GRCh38#1485204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155835862-A-C

1485204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835862-A-G

1485207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835859-T-G

1485331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835754-C-T

1485338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835747-G-A

1485491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835631-G-T

1485507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835616-G-C

1485601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835500-C-T

1485656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835444-G-A

1485656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835444-G-C

http://identifiers.org/hco/1/GRCh38#1485772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155835389-C-A

1485772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155835389-C-T

http://identifiers.org/hco/1/GRCh38#1485881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155835269-C-A

1485881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155835269-C-G

1485881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155835269-C-T

1485902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155835242-T-C

1485902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155835242-T-G

http://identifiers.org/hco/1/GRCh38#1485917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155835231-C-A

1485943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155835218-G-C

1486239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834924-A-G

1486387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834819-G-A

http://identifiers.org/hco/1/GRCh38#1486529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155834726-A-C

1486529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834726-A-G

1486529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834726-A-T

1486717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834514-G-A

1486718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834513-G-C

1486718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834513-G-T

1486744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834487-T-C

1486745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834486-G-A

1486745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834486-G-C

1486745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834486-G-T

1486761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834470-G-T

http://identifiers.org/hco/1/GRCh38#1486773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155834458-C-A

1486773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834458-C-T

1486781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834450-T-C

1486781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834450-T-G

1486791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834440-G-A

1486791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834440-G-C

1486791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834440-G-T

1486806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834436-G-A

http://identifiers.org/hco/1/GRCh38#1486812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155834430-C-A

1486812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155834430-C-T

1489110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155833294-G-A

1489110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155833294-G-C

1489145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155833260-C-T

1489162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155833243-G-C

1489174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155833227-G-T

1489186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155833215-G-T

http://identifiers.org/hco/1/GRCh38#1489190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155833210-C-A

1489190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155833210-C-T

1489240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155833160-G-A

1489240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155833160-G-T

1489279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155833121-G-A

1489279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155833121-G-C

1489308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155833094-C-T

1489310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155833092-G-T

1489319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155833078-A-G

1489320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155833077-G-A

1490680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155830475-G-C

1494206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155826972-C-T

1495884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825397-G-A

1495884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825397-G-T

1495897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825376-G-A

1495897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825376-G-C

1495897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825376-G-T

http://identifiers.org/hco/1/GRCh38#1495916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155825357-A-C

1495916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825357-A-G

http://identifiers.org/hco/1/GRCh38#1495938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155825334-C-A

1495938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825334-C-G

http://identifiers.org/hco/1/GRCh38#1495962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155825323-C-A

1495962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825323-C-G

1495976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825309-G-A

1495976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825309-G-T

http://identifiers.org/hco/1/GRCh38#1496070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155825226-A-C

1496070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825226-A-G

http://identifiers.org/hco/1/GRCh38#1496096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155825188-C-A

1496096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825188-C-T

1496113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825176-G-A

1496113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825176-G-T

http://identifiers.org/hco/1/GRCh38#1496134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155825154-A-C

1496134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825154-A-T

http://identifiers.org/hco/1/GRCh38#1496141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155825147-C-A

1496141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825147-C-G

1496141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825147-C-T

1496144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825144-T-C

1496210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825108-G-A

1496210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825108-G-C

1496210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825108-G-T

1496211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825107-T-C

1496226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825095-A-G

1496226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825095-A-T

1496255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24007
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155825062-G-T