49414883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244558-G-A

http://identifiers.org/hco/22/GRCh38#49414940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88244615-A-C

49414940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244615-A-G

49414958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244632-T-A

49414970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244644-C-T

49415014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244687-G-T

http://identifiers.org/hco/22/GRCh38#49415017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88244690-C-A

49415017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244690-C-G

49415017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244690-C-T

http://identifiers.org/hco/22/GRCh38#49415043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88244712-C-A

49415043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244712-C-T

49415070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244776-C-T

http://identifiers.org/hco/22/GRCh38#49415202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88244906-C-A

49415202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244906-C-T

49415225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244929-T-C

49415228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244932-T-C

http://identifiers.org/hco/22/GRCh38#49415234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88244938-C-A

49415234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244938-C-G

49415234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88244938-C-T

http://identifiers.org/hco/22/GRCh38#49415242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88244946-C-A

http://identifiers.org/hco/22/GRCh38#49415367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88245065-C-A

49415367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245065-C-G

49415367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245065-C-T

http://identifiers.org/hco/22/GRCh38#49415590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88245288-C-A

49415592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245290-G-T

49415843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245477-A-G

49415843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245477-A-T

49415921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245529-T-C

http://identifiers.org/hco/22/GRCh38#49415951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88245557-C-A

49415951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245557-C-T

http://identifiers.org/hco/22/GRCh38#49415988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88245593-C-A

http://identifiers.org/hco/22/GRCh38#49415994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88245599-C-A

49415994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88245599-C-T

49416512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88245669-G-T

49416523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88245680-G-T

49416536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88245693-A-G

49416674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88245833-G-A

49416674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88245833-G-T

49416677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88245836-G-A

49416677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88245836-G-T

49416715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88245876-C-T

49416752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88245912-C-T

49416856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: non coding transcript exon variant
orthologous variants: 88246005-C-T

49417030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246165-T-A

49417030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246165-T-G

http://identifiers.org/hco/22/GRCh38#49417111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88246230-C-A

49417174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246257-C-T

49417640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246627-C-T

49417775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246754-C-T

49417779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246758-G-A

49417810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246794-C-T

49417826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246813-T-A

49417926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246909-G-C

49417944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88246927-G-A

49418047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247026-G-A

http://identifiers.org/hco/22/GRCh38#49418454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88247406-C-A

49418454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247406-C-T

49418484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247439-G-A

49418484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247439-G-C

49418506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247468-G-C

49418519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247481-G-A

49418519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247481-G-T

49418588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247544-G-C

49418619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247584-G-A

49418692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88247647-G-A

http://identifiers.org/hco/22/GRCh38#49418907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88247866-A-C

49419233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248145-G-A

49419422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248291-G-T

49419436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248309-A-G

49419575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248448-A-T

49419581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248454-A-G

49419643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248512-A-G

49420694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88250389-G-A

49420694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88250389-G-T

49420841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88250556-G-A

49420857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88250572-A-G

49423706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88256007-G-A

49423733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88256034-G-C

49423733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88256034-G-T

http://identifiers.org/hco/22/GRCh38#49423918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88256215-C-A

49423974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88256280-T-G

49425964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88256929-G-A

49426167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257124-G-A

49426292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257249-A-G

49426298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257255-C-T

49426314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257273-C-T

49426321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257280-C-G

49426321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257280-C-T

49426431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257380-C-T

49426624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257508-G-A

49426628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257512-G-A

49426628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257512-G-C

49426636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257520-A-G

49426969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257590-G-T

http://identifiers.org/hco/22/GRCh38#49427025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88257646-A-C

49427033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257654-A-G

49427052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257673-T-C

49427056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257677-T-A

49427057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257678-G-T

http://identifiers.org/hco/22/GRCh38#49427070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88257692-C-A

49427115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257733-C-T

49427148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88257766-A-G

49427244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88258155-G-C

49427263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88258168-T-C

49427439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88258341-C-T

49432789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88265740-G-A

49432805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88265762-A-G

49432816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88265773-T-C

49432989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88265938-C-G

49432989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88265938-C-T

http://identifiers.org/hco/22/GRCh38#49433000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88265949-C-A

49433136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266000-A-G

49433152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266016-G-A

49433152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266016-G-T

49433165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88266029-T-G

49435503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88267745-C-T

49435519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88267761-A-G

49435536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88267778-C-T

49436879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88270886-T-C

49437295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88271288-G-A

49439678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278587-T-C

49439721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278623-C-T

49439722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278624-C-T

http://identifiers.org/hco/22/GRCh38#49448445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88284847-C-A

49448708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285112-C-T

49448784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285181-G-A

49448784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285181-G-C

49448784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285181-G-T

http://identifiers.org/hco/22/GRCh38#49448794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88285191-C-A

49448794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285191-C-T

49448831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285223-A-G

49448873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285268-C-T

49448909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285301-A-G

49448915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285307-T-A

49448963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285362-C-T

49449561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285534-G-C

49449569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285548-G-T

http://identifiers.org/hco/22/GRCh38#49450029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88285920-C-A

49450029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285920-C-G

49450173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286066-G-A

49450190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286087-T-C

49450232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286126-C-T

49453092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286923-G-A

49453115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286946-C-G

49453119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286950-A-G

49453204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286999-A-G

49453204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286999-A-T

49453215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88287010-A-G

49453237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88287034-G-A

49453306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88287100-T-C

49453307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88287101-G-A

49453332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88287126-A-G

49453501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88287277-G-A

49453582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88287358-T-C

49454300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88288029-G-A

49455745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88288311-C-T

49455811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88288367-G-C

49455924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88288456-G-A

49456174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88288652-C-T

49456202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88288670-T-A

49456287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88288753-A-T

49460455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88292528-G-A

49460673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88292737-T-C

49461024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293069-G-A

http://identifiers.org/hco/22/GRCh38#49461046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88293091-C-A

49461237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293282-G-A

49461273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293325-G-C

49461293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293345-C-G

49461364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293419-G-A

49461388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293426-G-A

49461388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293426-G-C

49461413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293448-G-C

49461806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294565-G-A

49461838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294596-G-C

49461864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294617-G-A

49461979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294727-G-A

49462054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294788-G-A

49462054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294788-G-T

49462055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294789-G-A

49462055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294789-G-C

49462073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294805-G-A

49462140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294870-G-C

49462347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88295049-T-C

49468069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88298859-G-A

49468070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88298860-G-C

49468133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88298922-G-C

49468209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299002-A-G

49468291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299087-C-T

49468645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299395-A-G

49468648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299398-C-G

49468650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299400-A-G

49468687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299451-G-T

49468765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299522-G-C

49468890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299655-C-T

49468901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299666-G-A

49468930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299695-T-C

49471149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88301940-G-C

49471211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88302000-A-T

49471448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88302235-T-C

49472215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88303165-C-T

49472675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88303473-G-A

49472688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88303486-C-T

49472817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88303615-A-T

49473040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88303837-G-C

49473385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88304166-G-A

49473471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88304268-T-C

49474085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88304992-C-T

49474413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305256-A-G

http://identifiers.org/hco/22/GRCh38#49474495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88305337-A-C

49474495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305337-A-T

49474555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305395-G-A

49474628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305452-T-C

49474645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305469-A-G

49476803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88308961-G-A

49477124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309278-G-A

49477196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309346-G-A

49477248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309398-T-A

49477248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309398-T-G

49477272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309443-G-A

49477272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309443-G-C

49477364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309539-T-C

49477428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309621-G-T

49477490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309698-G-C

49477506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309714-T-A

49477534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309745-T-A

49477534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309745-T-G

49477538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309749-G-T

49477587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309803-A-G

49477587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309803-A-T

49477672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309889-A-G

49477681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309898-T-G

49477745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88309979-G-A

49477805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310040-G-A

49477805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310040-G-C

49477807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310042-T-A

49477965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310251-T-G

49478484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310753-T-A

49479622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310829-C-T

49479653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310858-T-A

49479653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310858-T-C

49479884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311094-C-T

49480199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311437-T-A

http://identifiers.org/hco/22/GRCh38#49480261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88311499-C-A

49480344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311563-G-A

49480511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311681-G-A

49480553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311723-G-C

49480659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311816-T-C

49480727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311882-T-C

49481763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312635-G-A

49481764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312636-C-G

49481770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312642-G-A

49481809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312680-G-A

49482085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312856-A-G

49482125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312907-G-T

49482145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312929-G-A

49482145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312929-G-T

49482153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312937-C-T

49482231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88313012-G-A

49482285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88313075-G-C

49482302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88313100-C-T

49482733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88313519-C-T

49482806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88313587-T-A

49483318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315439-G-C

49483439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315570-G-A

http://identifiers.org/hco/22/GRCh38#49483735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88315860-A-C

49483764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315887-G-A

49483780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315903-C-T

49483845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315968-C-T

http://identifiers.org/hco/22/GRCh38#49487830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88318116-A-C

http://identifiers.org/hco/22/GRCh38#49488230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88318477-A-C

http://identifiers.org/hco/22/GRCh38#49488373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#88318678-C-A

49488472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88318767-G-T

49488747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319022-G-A

49488986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319242-C-T

49489329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319565-G-A

49489329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319565-G-T

49492741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88326919-C-T

49492783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88326964-G-A

49493281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88327456-T-C

49493475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88327633-T-C

49499549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328336-C-G

49499584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328372-C-T

49499644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328417-T-C

49499707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328476-T-G

49499716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328485-G-T

49500004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328746-G-C

49500014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328766-G-C

49500250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329046-T-A

49500260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329063-C-T

49500317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329123-G-T

49500326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329131-G-C

49500337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329143-G-A

49500350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329155-G-A

http://identifiers.org/hco/22/GRCh38#49500362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88329167-A-C

49500371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329175-G-C

49500375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329179-G-T

49500384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329187-G-A

49500466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329270-T-C

http://identifiers.org/hco/22/GRCh38#49501127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88331656-C-A

http://identifiers.org/hco/22/GRCh38#49501166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88331699-C-A

49501166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88331699-C-T

http://identifiers.org/hco/22/GRCh38#49501281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88331815-C-A

49501281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88331815-C-T

http://identifiers.org/hco/22/GRCh38#49501339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88331873-C-A

49501347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88331881-C-T

49501406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88331928-T-C

49501416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88331941-C-T

49501542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88332068-C-T

49501692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332219-A-G

49501708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332235-T-C

49502008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332536-T-C

49502026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332555-T-C

49502362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88332912-G-A

49502362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88332912-G-T

49503128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88333673-A-T

http://identifiers.org/hco/22/GRCh38#49503252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88333805-C-A

49503283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88333838-G-A

49503889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88334595-A-G

49503899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88334603-C-T

49504140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88334820-A-G

49504326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88334991-T-C

49504562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335195-C-G

49504606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335230-C-T

49504663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335289-T-A

49504855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335472-C-T

49504967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335579-A-G

http://identifiers.org/hco/22/GRCh38#49505050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88335695-A-C

49505158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335767-G-A

49505218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335828-G-A

49505224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335834-G-T

49505292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335906-A-T

49512085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88339695-T-C

49512844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88340386-G-A

49512925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88340477-T-C

49513097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88340623-C-T

49513132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88340644-C-T

49514702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352314-C-T

49514712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352329-C-G

49515448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353011-G-A

49515510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353062-C-T

http://identifiers.org/hco/22/GRCh38#49515795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88353296-A-C

49515814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353315-C-T

49515874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353352-T-A

49517008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354465-C-G

49517107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354552-G-T

49517198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354676-C-T

49517200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354678-C-T

49517232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354706-C-T

49517251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354727-C-G

49517271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354747-C-T

49518267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88355033-G-A

49524605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88357439-A-T

49524615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88357449-C-T

49526652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88359372-T-G

49526706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88359425-C-T

49526941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88359655-G-T

49527083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88359784-T-C

http://identifiers.org/hco/22/GRCh38#49533893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88361672-A-C

49533921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88361702-C-T

49533980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88361743-G-A

49533980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88361743-G-C

49533980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88361743-G-T

http://identifiers.org/hco/22/GRCh38#49534280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88362410-C-A

49534280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362410-C-T

49534297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362427-T-C

49534309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362436-T-C

49534309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362436-T-G

49534320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362447-G-T

49534447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362577-C-T

http://identifiers.org/hco/22/GRCh38#49534448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88362578-C-A

49534510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362623-G-A

49534510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362623-G-C

49534591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362696-G-A

http://identifiers.org/hco/22/GRCh38#49534606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88362711-C-A

49534745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88362853-A-G

49534954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88363025-C-T

49535180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88363235-G-A

49535186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88363241-G-A

49535186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88363241-G-T

49538398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88365655-T-C

49538491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88365749-A-G

http://identifiers.org/hco/22/GRCh38#49538749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88365990-C-A

http://identifiers.org/hco/22/GRCh38#49539079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88366254-C-A

49539223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366377-T-C

49539389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366554-C-T

49539497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366664-G-A

49539812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366923-C-T

49539878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366996-C-G

49539878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366996-C-T

49539879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366997-G-A

49539879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88366997-G-T

49552281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88368307-G-A

49552447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88368512-A-T

http://identifiers.org/hco/22/GRCh38#49552533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88368604-C-A

49552533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88368604-C-T

49552535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88368606-G-A

49552535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88368606-G-T

49552555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88368622-G-T

49552637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88368698-A-G

49552644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88368705-T-C

49552665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88368726-G-A

49552666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88368727-G-A

49552666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88368727-G-T

49561255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380757-G-A

49561294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380792-G-A

49561373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380855-A-G

49561434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380911-G-C

49561679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381144-C-G

49561768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381232-G-A

49561838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381292-A-G

49561980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381433-A-G

49562000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381454-C-T

49562004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381458-G-A

49562022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381476-C-T

49562156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381609-C-T

49562192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381644-G-A

49562324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381756-C-T

49562364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381797-C-G

http://identifiers.org/hco/22/GRCh38#49572138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88386363-C-A

49572138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386363-C-T

49572208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386433-A-G

49572399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386610-A-G

49572455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386654-C-G

49572455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386654-C-T

49572545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386740-T-C

49572683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386860-A-G

49572683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386860-A-T

49572733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386910-T-C

49572763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386929-G-A

49572763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386929-G-T

49572764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386930-C-T

49572772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386938-A-G

http://identifiers.org/hco/22/GRCh38#49572780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88386948-C-A

http://identifiers.org/hco/22/GRCh38#49572793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88386961-A-C

49572825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88386993-G-T

49573426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389167-T-G

49573430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389171-G-A

49573430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389171-G-T

49573439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389176-A-G

49573479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389214-A-G

49573523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389252-A-G

49573585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389307-G-T

http://identifiers.org/hco/22/GRCh38#49573612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88389324-C-A

49573614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389326-C-T

49573620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389332-G-A

49573637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389350-G-C

http://identifiers.org/hco/22/GRCh38#49573646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88389359-C-A

49573646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389359-C-T

49573650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389363-A-G

49574454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389800-G-A

49574454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389800-G-T

http://identifiers.org/hco/22/GRCh38#49574536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88389900-C-A

49574554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88389917-T-C

http://identifiers.org/hco/22/GRCh38#49574579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88389942-C-A

49574782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390147-T-C

49575086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390412-G-A

49575086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390412-G-T

49588387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88396453-C-T

49588789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88396858-T-C

49613643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88415847-T-C

49613660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88415864-G-A

49613660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88415864-G-T

49613669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88415873-C-T

49613674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88415878-C-T

http://identifiers.org/hco/22/GRCh38#49613677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88415881-C-A

49613744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88415950-C-T

49613769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88415974-C-T

http://identifiers.org/hco/22/GRCh38#49613797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88416001-C-A

49613836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416039-G-A

49613902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416091-G-A

49613902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416091-G-C

49613928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416121-G-A

http://identifiers.org/hco/22/GRCh38#49613932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88416125-C-A

49613932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416125-C-T

49613933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416126-G-A

49613933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416126-G-T

49613996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416175-A-G

49614001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416180-T-C

49614080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416219-G-A

49614094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416233-C-T

49614095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416234-G-A

http://identifiers.org/hco/22/GRCh38#49614126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88416269-C-A

49614258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416375-A-T

49614297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416414-C-T

49614347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416471-A-G

49614595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416709-T-G

49614639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88416753-G-A

49614869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417000-G-A

49614869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417000-G-T

http://identifiers.org/hco/22/GRCh38#49614915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88417042-A-C

49614915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417042-A-G

49614977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417121-T-C

49615038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417185-G-A

49615038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417185-G-C

49615038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417185-G-T

http://identifiers.org/hco/22/GRCh38#49615130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88417256-C-A

49615130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417256-C-T

49620422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417790-G-A

49620422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417790-G-C

49620422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417790-G-T

49620520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417910-G-A

49620520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88417910-G-T

49620675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418070-A-G

http://identifiers.org/hco/22/GRCh38#49620687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88418082-C-A

49620687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418082-C-G

49620687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418082-C-T

49620692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418087-A-T

49621107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418496-A-T

49621270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418659-T-C

49621307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418696-T-C

49621386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418777-G-C

http://identifiers.org/hco/22/GRCh38#49621405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88418796-C-A

49621405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418796-C-T

49621447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418834-T-G

49621486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418865-G-C

http://identifiers.org/hco/22/GRCh38#49630900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88420434-C-A

49630916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88420450-T-C

49631321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88420812-T-A

http://identifiers.org/hco/22/GRCh38#49632426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88421296-C-A

49632541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88421415-G-A

49632542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88421416-G-A

49632713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88421592-G-A

http://identifiers.org/hco/22/GRCh38#49632717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#88421596-C-A

49632717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88421596-C-T

http://identifiers.org/hco/22/GRCh38#49632899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#88421742-C-A

49632958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88421809-T-C

49633038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88421887-C-G

49633038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88421887-C-T

49633045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88421894-G-A

49635510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88433956-A-G

49635831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88434287-G-T

49645444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88436875-T-G

49645727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88437085-C-G

49645878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88437213-T-C

49646007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88437322-G-A

49646072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88437388-A-G

49646154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88437479-A-G

49648474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88444909-C-G

49648588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88445016-C-T

49649928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88445829-C-T

http://identifiers.org/hco/22/GRCh38#49650322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88446177-C-A

http://identifiers.org/hco/22/GRCh38#49650353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88446217-C-A

49650353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446217-C-T

49650356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446220-A-G

49650519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446392-G-A

49650545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446419-G-A

49650555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446426-G-A

49650555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446426-G-C

49650684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446594-A-G

49650691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446601-T-C

49650703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446613-C-G

49650731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446638-T-G

49650924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446881-A-G

49650924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446881-A-T

49650952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88446911-C-T

http://identifiers.org/hco/22/GRCh38#49651170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88447091-C-A

http://identifiers.org/hco/22/GRCh38#49651248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#88447173-A-C

49651264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88447189-C-T

49651341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88447260-A-G

49655600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88448894-T-C

49655805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88449083-C-T

49655868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88449192-T-C

49655884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28010
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88449208-A-G