89254669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100489-T-C

89254702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100454-T-C

89254780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100420-C-T

89254785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100415-T-C

89254834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100375-A-T

http://identifiers.org/hco/6/GRCh38#89254866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33100344-C-A

89255095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100142-A-G

89255473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100108-G-A

89255475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33100106-C-G

89255608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33099980-A-T

89255658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3 prime UTR variant
orthologous variants: 33099947-T-C

89257220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095977-T-A

89257228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095969-T-G

89257297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095910-T-C

http://identifiers.org/hco/6/GRCh38#89257435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33095778-C-A

89257435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095778-C-T

89257458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095755-G-A

89257458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095755-G-T

89257468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095745-G-A

89257468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095745-G-T

89257480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095733-G-A

89257480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095733-G-T

89257516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095699-T-A

http://identifiers.org/hco/6/GRCh38#89257518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33095697-C-A

89257518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095697-C-G

89257518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095697-C-T

89257635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095618-G-A

89257635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095618-G-T

89257663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095590-G-A

89257663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095590-G-C

89257664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33095589-G-T

http://identifiers.org/hco/6/GRCh38#89257770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33095483-C-A

89257770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33095483-C-G

89257770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33095483-C-T

89257944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33095309-A-G

http://identifiers.org/hco/6/GRCh38#89257970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33095283-C-A

89257970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33095283-C-T

89258000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33095253-A-G

89258007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33095246-T-C

89258023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33095231-G-A

89258023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33095231-G-T

89258082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33095172-G-T

89258131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33095124-T-C

89264345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085811-G-A

89264345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085811-G-C

89264345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085811-G-T

http://identifiers.org/hco/6/GRCh38#89264373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33085781-C-A

89264373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085781-C-G

89264373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085781-C-T

89264696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085460-T-C

http://identifiers.org/hco/6/GRCh38#89264746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33085411-C-A

89264746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085411-C-T

89264750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085407-G-C

89264750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085407-G-T

89265006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085195-G-A

89265469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084814-T-C

89265478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084805-G-T

89265491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084793-G-A

89265491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084793-G-T

89265543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084736-T-C

89265559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084569-A-G

89265559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084569-A-T

89265603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084515-A-G

89265666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33084452-G-T

89267653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082712-A-G

89267657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082708-G-T

89267659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082706-T-C

89267753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33082612-T-C

89267756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33082609-T-C

89268004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082369-T-G

89268043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33082330-G-A

89268043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33082330-G-T

89268109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082264-G-A

89268109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082264-G-T

89268141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082233-G-T

89268164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082211-A-G

89268184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082190-G-A

89268184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082190-G-T

89268187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082185-T-A

89268187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082185-T-C

http://identifiers.org/hco/6/GRCh38#89268194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33082178-C-A

89268194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082178-C-T

89268198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082174-T-A

89268198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082174-T-C

89268198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082174-T-G

89268255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082124-A-G

89268302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082089-A-G

89268302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33082089-A-T

89268424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33081969-G-A

89268725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33081770-A-G

89268737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33081758-T-C

89268921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33081611-A-T

89268955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33081575-G-T

89269001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33081560-A-G

89269044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33081517-A-G

89269246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081317-G-A

89269246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081317-G-C

89269248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081315-G-A

89269260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081292-C-G

89269260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081292-C-T

89269276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081276-G-A

89269276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081276-G-C

89269276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081276-G-T

http://identifiers.org/hco/6/GRCh38#89269286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33081266-C-A

89269286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081266-C-T

89269318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081236-G-T

http://identifiers.org/hco/6/GRCh38#89269332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33081222-C-A

89269332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33081222-C-T

89269380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33081164-G-A

89269380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33081164-G-T

89269612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33080257-T-C

89269722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33080144-C-G

89269807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33080068-T-C

http://identifiers.org/hco/6/GRCh38#89269906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33079897-A-C

89269943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33079854-G-C

http://identifiers.org/hco/6/GRCh38#89269986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33079811-A-C

89270078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33079737-A-G

89270236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33079602-G-A

89270236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33079602-G-T

89270246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33079592-A-G

89270356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33079461-T-C

89270470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33078852-A-G

89270574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33078759-C-T

http://identifiers.org/hco/6/GRCh38#89270589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33078744-C-A

89270589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33078744-C-T

http://identifiers.org/hco/6/GRCh38#89270591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33078742-C-A

89270621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33078713-G-A

89270895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33078178-G-T

89270975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33078103-A-G

89271020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33078060-T-A

89271212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077886-G-A

89271258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077848-G-C

89271258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077848-G-T

89271548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077625-A-G

89271583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077600-G-T

89271589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077594-G-A

89271589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077594-G-T

http://identifiers.org/hco/6/GRCh38#89271612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33077571-C-A

89271612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077571-C-T

89271613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077570-A-G

http://identifiers.org/hco/6/GRCh38#89271627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33077549-C-A

89271627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 33077549-C-T

http://identifiers.org/hco/6/GRCh38#89271787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33077388-C-A

89271793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077385-G-T

http://identifiers.org/hco/6/GRCh38#89271801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33077377-C-A

89271803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077375-G-A

89271803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077375-G-C

89271803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077375-G-T

89271804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077374-G-A

89271808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077370-G-C

89271808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077370-G-T

89271838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077339-T-C

89271844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077333-T-C

89271881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077293-G-A

89271889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33077282-G-T

89272011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077163-C-T

89272019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077155-G-A

89272022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077152-G-A

89272055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33077112-C-G

89272302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33076964-A-G

89279078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33076247-C-T

http://identifiers.org/hco/6/GRCh38#89279135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33076190-C-A

89279135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33076190-C-T

89279165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33076160-G-A

http://identifiers.org/hco/6/GRCh38#89279171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33076154-C-A

89279358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33075935-A-T

89279375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33075918-G-A

89279375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33075918-G-C

89279399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33075894-G-A

89280288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33074993-T-A

89280288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33074993-T-G

89280368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33074914-C-G

89280526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33074762-G-A

http://identifiers.org/hco/6/GRCh38#89298301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33072630-C-A

89298301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33072630-C-T

89298736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33072174-A-G

89299669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33071527-G-A

89299676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33071520-T-C

89299812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33071401-T-C

89299858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33071355-A-G

89299860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33071353-A-G

89300063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071162-G-T

89306941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070604-T-C

89306942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070603-G-T

89307132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070433-A-T

89307175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070390-T-C

89308714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33069220-T-C

89308782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33069167-T-C

89308875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33069096-G-A

89308913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33069074-G-A

89309283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068863-G-A

89309283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068863-G-T

89309334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068827-A-G

89309481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068684-C-T

89309601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068558-T-C

89309625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068537-G-A

89309706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068469-G-A

http://identifiers.org/hco/6/GRCh38#89309720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33068455-A-C

89310090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068368-G-C

89310125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068351-G-A

89310338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068186-C-T

89310450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068074-C-T

89310469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33068057-G-C

89310792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33067817-A-G

89311045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33067553-G-A

89311050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33067548-T-A

http://identifiers.org/hco/6/GRCh38#89311146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#33067485-A-C

89311166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33067474-G-A

89311166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33067474-G-C

89311351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33066335-C-T

89311356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33066330-C-T

89311374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33066309-C-G

89311374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33066309-C-T

89312076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33065660-G-T

89312295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33065524-T-G

http://identifiers.org/hco/6/GRCh38#89312394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33065424-C-A

89312454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33065371-G-A

89312512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33065311-G-A

89312781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33065225-C-T

89312829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33065183-C-T

http://identifiers.org/hco/6/GRCh38#89312943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33065072-C-A

89312943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33065072-C-T

89313001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33065022-G-A

89313490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33064640-C-T

89313551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33064591-G-A

89314044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33064461-T-A

http://identifiers.org/hco/6/GRCh38#89314113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33064394-C-A

89314115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33064392-T-C

http://identifiers.org/hco/6/GRCh38#89314331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33064108-A-C

89314755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33063611-A-G

89314824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33063557-C-G

89314824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33063557-C-T

89314825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33063556-G-A

89315172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33063245-G-A

89315172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33063245-G-C

89315246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33063170-C-T

http://identifiers.org/hco/6/GRCh38#89315252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#33063164-C-A

89315252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4091
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33063164-C-T