112394975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104961602-G-C

http://identifiers.org/hco/1/GRCh38#112395203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104961183-C-A

112395518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, undefined
orthologous variants: 104960930-G-C

112395612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104960831-G-A

112395743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, undefined
orthologous variants: 104960707-A-G

112395907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, undefined
orthologous variants: 104960561-T-A

http://identifiers.org/hco/1/GRCh38#112396134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104960360-C-A

112396134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104960360-C-T

112396142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104960352-G-T

112396310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104960177-G-A

112396345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104960142-G-A

112396345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104960142-G-T

112396352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104960135-T-C

112396421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104960066-T-C

http://identifiers.org/hco/1/GRCh38#112396433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104960054-C-A

112396563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104959928-G-T

http://identifiers.org/hco/1/GRCh38#112396617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104959877-C-A

112396617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104959877-C-G

112396641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104959853-A-G

112396908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104959581-G-T

112397232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104959276-A-G

112397697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104958813-C-T

112397701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104958809-C-T

112397706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104958804-T-C

112397821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104958703-G-T

112398196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104958317-G-C

112398207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104958301-A-G

112398520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104957858-C-G

http://identifiers.org/hco/1/GRCh38#112398859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104957694-C-A

112399035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104957538-T-A

112400994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104956427-T-A

http://identifiers.org/hco/1/GRCh38#112401404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104955746-C-A

112401740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104955499-A-G

112402547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104954856-A-T

112402750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104954609-A-G

http://identifiers.org/hco/1/GRCh38#112403901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104953807-C-A

112403908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104953800-A-G

112404034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104953666-A-G

112404348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104953471-A-G

112404398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, undefined
orthologous variants: 104953426-G-A

112404440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104953385-A-G

112404566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104953273-T-C

112405223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104953007-C-G

112405332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104952915-C-G

112405451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104952811-C-T

112405683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104952715-T-A

112406389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104952176-G-A

112406760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104951878-T-C

112406907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104951755-T-A

112407567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104950110-C-G

112409332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104948984-A-G

112409791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104948561-C-T

112410208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104948177-C-G

112410234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104948149-A-G

http://identifiers.org/hco/1/GRCh38#112410294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104948076-A-C

http://identifiers.org/hco/1/GRCh38#112410369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104948022-C-A

112410444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104947947-G-T

112410457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104947934-T-C

112411086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104947325-G-A

112411133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104947278-T-C

112411133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104947278-T-G

112411671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104946763-C-G

112411679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104946755-A-G

112411706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104946740-G-A

112411706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104946740-G-T

112411722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 104946724-G-A

112412290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 5 prime UTR variant
orthologous variants: 104946204-A-T

112412528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104945990-A-G

112412534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104945984-C-G

112413107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104945407-A-G

112413113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104945401-A-G

112414351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104943599-G-A

112414454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104943499-A-G

http://identifiers.org/hco/1/GRCh38#112414526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104943424-C-A

112414693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104943280-A-G

http://identifiers.org/hco/1/GRCh38#112414696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104943277-C-A

112414884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104941035-T-C

112415177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104940731-C-G

http://identifiers.org/hco/1/GRCh38#112415195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104940700-C-A

112415195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104940700-C-G

112415258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104940628-A-G

112415278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104940607-T-A

http://identifiers.org/hco/1/GRCh38#112415296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104940589-A-C

112415296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104940589-A-G

112415857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104940342-A-G

112415895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104940315-T-G

http://identifiers.org/hco/1/GRCh38#112416063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104940159-C-A

112416063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104940159-C-T

112416124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104940104-T-G

http://identifiers.org/hco/1/GRCh38#112416296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104939931-C-A

112416302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104939925-T-C

112416304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104939923-G-A

112416304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104939923-G-T

112416325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104939904-T-A

112416325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104939904-T-C

112418389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934845-T-G

112418456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934783-A-G

112418503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934737-A-G

112418667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934583-A-G

112418701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934563-G-A

112418701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934563-G-C

112418899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934359-A-G

112418929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104934340-T-A

112429452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104931745-T-C

112429932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104931384-C-G

112429961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104931352-A-G

112430067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104931247-T-C

112430127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104931188-A-G

112430127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104931188-A-T

112430901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104931146-A-G

112431322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104930770-T-C

http://identifiers.org/hco/1/GRCh38#112435248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104928191-A-C

112435248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104928191-A-G

112435372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104928063-A-G

http://identifiers.org/hco/1/GRCh38#112435408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104928027-A-C

112435408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104928027-A-G

112435425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104928011-G-A

112435658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104927798-T-C

http://identifiers.org/hco/1/GRCh38#112435817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104927437-A-C

112439621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925773-C-T

112439694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925707-A-G

112439727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925678-A-T

112439991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925416-G-A

112440065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925344-C-G

112440281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925195-C-G

112440311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925178-C-T

112440334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925154-A-G

112440363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925129-G-T

112440506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104925001-C-T

112440530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104924973-G-A

http://identifiers.org/hco/1/GRCh38#112442493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104922621-C-A

112442493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104922621-C-G

112442493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104922621-C-T

112442612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104922508-T-A

112444370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104921611-G-T

112444398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104921586-C-T

112444566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104921426-G-C

112444566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104921426-G-T

http://identifiers.org/hco/1/GRCh38#112445718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104920615-A-C

112447974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104919714-G-A

112448020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104919664-G-A

112448316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104919447-A-G

112448877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104918793-T-C

112449095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104918584-G-A

112449128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104918551-C-T

112449149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104918530-G-A

112449149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104918530-G-C

112449228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104918465-T-C

112449228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104918465-T-G

112449258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104918438-A-G

112449258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104918438-A-T

http://identifiers.org/hco/1/GRCh38#112449317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104918379-C-A

112450098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104917815-G-A

112450308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104917617-A-G

112453905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104915851-A-G

112454280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104915509-C-G

112454280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104915509-C-T

112454455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: synonymous variant
orthologous variants: 104915363-C-T

112454559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104915259-A-G

112455697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104913692-A-G

http://identifiers.org/hco/1/GRCh38#112455808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104913597-C-A

112455808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104913597-C-T

112455850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104913552-T-A

112455850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104913552-T-C

112455882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104913520-T-C

http://identifiers.org/hco/1/GRCh38#112455883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104913519-A-C

112455883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104913519-A-G

112455883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron variant
orthologous variants: 104913519-A-T

112455940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: stop gained
orthologous variants: 104913433-G-T

http://identifiers.org/hco/1/GRCh38#112456088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104913285-A-C

112456111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: synonymous variant
orthologous variants: 104913262-T-C

112456111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104913262-T-G

112456222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104913151-A-G

112456222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104913151-A-T

112456327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104913046-G-C

112456327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104913046-G-T

112456528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104912845-G-T

112456592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104912781-A-G

112456592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104912781-A-T

112456727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: stop gained
orthologous variants: 104912646-C-G

112456727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense variant
orthologous variants: 104912646-C-T

112456900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104912473-G-A

112456975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104912398-T-C

112456996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104912377-C-G

112456996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 104912377-C-T

112457047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104912329-A-G

112457230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104912146-C-G

http://identifiers.org/hco/1/GRCh38#112457484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104911890-C-A

112457653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104911717-G-T

112457671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104911699-T-C

112457690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104911677-G-A

112457690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104911677-G-C

112457690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104911677-G-T

112457993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104911375-A-G

112458463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104910972-C-T

112458810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104910738-A-G

112459103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104910509-T-C

112459205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104910408-A-G

112459266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104910350-G-A

112459266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104910350-G-T

112459287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104910329-G-A

112459565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909874-T-C

112459617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909835-G-A

112459638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909814-G-T

112459639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909813-G-A

112459639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909813-G-T

112459667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909785-G-T

112459816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909639-T-G

112460138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104909317-A-G

http://identifiers.org/hco/1/GRCh38#112460550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104908252-A-C

112460635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104908172-T-G

http://identifiers.org/hco/1/GRCh38#112460752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104908045-C-A

http://identifiers.org/hco/1/GRCh38#112460877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104907797-C-A

112460877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104907797-C-T

112461185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104907425-C-T

112461193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104907412-T-C

112461335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104907293-T-G

112461357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104907273-A-G

112461371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104907261-G-A

http://identifiers.org/hco/1/GRCh38#112461381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104907251-A-C

112461406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104907230-G-C

112461572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104907074-A-G

112461680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104905101-G-A

112461680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104905101-G-T

112462450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104904618-G-T

http://identifiers.org/hco/1/GRCh38#112462513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104904564-C-A

112462513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104904564-C-T

112462618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904515-A-G

112462646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904487-G-T

http://identifiers.org/hco/1/GRCh38#112462703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104904446-C-A

112462703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904446-C-G

112462703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904446-C-T

http://identifiers.org/hco/1/GRCh38#112462756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104904426-C-A

112462766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904416-A-G

112462767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904415-A-G

112462879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904316-T-G

112462901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904295-A-G

112462908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904288-T-C

http://identifiers.org/hco/1/GRCh38#112462974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#104904228-C-A

112462974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904228-C-T

112462975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904227-T-C

112463024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25330
most severe consequence: non coding transcript exon variant
orthologous variants: 104904199-G-T