111092325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non coding transcript exon variant
orthologous variants: 32970319-T-G

111092347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non coding transcript exon variant
orthologous variants: 32970341-T-G

111092363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32970357-C-G

111092363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32970357-C-T

http://identifiers.org/hco/5/GRCh38#111092381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32970373-A-C

111092381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32970373-A-G

111092420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32970413-A-G

111092420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32970413-A-T

111092468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32970461-C-G

111092678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970653-T-C

111092760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970737-A-G

111092764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970741-G-A

111092764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970741-G-T

111092906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970868-T-G

111093412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971233-C-T

111093473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971274-T-C

111093474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971275-T-G

111093546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971335-G-A

http://identifiers.org/hco/5/GRCh38#111093787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32971547-C-A

111093814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971574-A-G

http://identifiers.org/hco/5/GRCh38#111093915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32971646-A-C

111093915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971646-A-G

111093915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971646-A-T

111093922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971653-A-G

111093937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971684-G-A

111093966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971702-C-G

111093966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971702-C-T

111094026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971753-T-A

111094077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971804-C-G

111094184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971905-A-G

111094868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972424-A-G

111094868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972424-A-T

111094874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972430-A-G

111094894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972454-T-G

111094895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972455-T-G

111094901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972461-T-A

111094901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972461-T-C

111094901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972461-T-G

111094940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32972505-T-C

111094940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32972505-T-G

http://identifiers.org/hco/5/GRCh38#111094977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32972540-C-A

111094977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32972540-C-T

http://identifiers.org/hco/5/GRCh38#111095005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32972573-A-C

111095005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32972573-A-G

111095273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972825-A-T

111095307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972854-G-A

111095307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972854-G-T

111095336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972860-T-C

http://identifiers.org/hco/5/GRCh38#111095474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32972964-C-A

111096042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973467-A-G

111096071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973499-G-A

111096071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973499-G-T

111096095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973523-G-A

111096121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973553-A-G

111096140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973573-T-A

111096202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973645-T-C

http://identifiers.org/hco/5/GRCh38#111096800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32973901-C-A

http://identifiers.org/hco/5/GRCh38#111096935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32973970-A-C

111096935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973970-A-G

111096947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973981-C-G

111096947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973981-C-T

111097003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974031-A-G

111097003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974031-A-T

111097037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32974065-T-A

111098196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974450-G-C

111098483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974719-C-G

http://identifiers.org/hco/5/GRCh38#111098587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32974822-C-A

111098587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974822-C-T

111098604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974835-T-A

111098676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974906-A-T

http://identifiers.org/hco/5/GRCh38#111098801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32975029-C-A

111098801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32975029-C-G

111098801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32975029-C-T

111098880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975099-A-G

http://identifiers.org/hco/5/GRCh38#111098918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32975148-A-C

111098918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975148-A-G

111098986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975207-A-G

111098986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975207-A-T

111099039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975252-A-G

111099060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975273-A-T

111099094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975305-T-C

111099344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975568-T-A

111099344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975568-T-G

111099347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975571-C-G

111099385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975611-A-G

http://identifiers.org/hco/5/GRCh38#111099437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#32975655-C-A

111099437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32975655-C-T

111099484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975705-T-C

111099526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975732-G-A

111099526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975732-G-T

111099747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975898-G-C

111100408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32976419-C-G

111100440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32976601-G-T

111100547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32976773-A-G

111100746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32976969-T-C

111101171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32977044-T-A

111101219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32977092-A-G

111101518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

111101608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

111101790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32977720-C-T

111101821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32977750-C-T

111102010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32978012-C-G

111102468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32978763-A-G

http://identifiers.org/hco/5/GRCh38#111102530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32978823-C-A

111102530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32978823-C-T

111102739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32978993-C-G

111102752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979006-T-C

111102752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979006-T-G

111102786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979039-T-C

111102864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979117-A-G

111102934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979155-A-G

111102945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979167-T-A

111102972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979194-C-G

http://identifiers.org/hco/5/GRCh38#111103009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32979231-A-C

111103056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979267-A-T

111103389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979537-C-T

111103479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979628-A-G

http://identifiers.org/hco/5/GRCh38#111103595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32979734-A-C

http://identifiers.org/hco/5/GRCh38#111103653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32979782-C-A

111103653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979782-C-G

111103685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32979815-T-A

111104346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32980364-T-C

http://identifiers.org/hco/5/GRCh38#111104441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32980444-C-A

111104441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32980444-C-G

111104444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32980447-G-A

111104480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32980481-G-A

http://identifiers.org/hco/5/GRCh38#111104600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32980559-A-C

111104600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32980559-A-G

111104600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32980559-A-T

111104617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32980573-G-T

111104711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32980656-T-C

111104718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32980663-A-G

111104759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32980704-T-C

111104763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32980708-C-T

http://identifiers.org/hco/5/GRCh38#111104875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32980817-C-A

http://identifiers.org/hco/5/GRCh38#111104896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32980842-C-A

111104896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32980842-C-T

111105855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32981962-T-G

111105933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982003-G-A

111105933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982003-G-T

111106001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982079-A-G

111106085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32982154-T-C

111106282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982312-G-A

111106282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982312-G-C

111106282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982312-G-T

111106333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982360-A-G

111106358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982378-T-C

http://identifiers.org/hco/5/GRCh38#111107168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32983284-C-A

111107168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983284-C-T

111107174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983290-G-C

111107206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983340-T-C

111107207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983341-A-G

http://identifiers.org/hco/5/GRCh38#111107264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32983410-A-C

111107264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983410-A-G

111107308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32983454-A-G

111107439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 32983588-A-T

111108338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32984290-A-G

111108442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32984393-A-T

111108513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32984461-A-G

111108566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32984508-A-T

111110165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985005-A-G

111110286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32985131-G-T

http://identifiers.org/hco/5/GRCh38#111110585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32985350-C-A

111110585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985350-C-T

111110638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985394-T-C

111110713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985470-A-T

111110792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32985542-C-G

111110792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32985542-C-T

111110816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32985566-A-G

111110849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32985599-T-G

111111002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985754-G-A

http://identifiers.org/hco/5/GRCh38#111111073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32985832-C-A

111111073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985832-C-T

http://identifiers.org/hco/5/GRCh38#111111074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32985833-C-A

111111086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985845-C-G

111111089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985848-G-T

111111148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985896-A-T

111111299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32986046-T-C

http://identifiers.org/hco/5/GRCh38#111111311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32986058-C-A

111111313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32986060-T-C

111111313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32986060-T-G

111111443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32986207-T-G

111111444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32986208-T-C

111111477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32986241-A-G

http://identifiers.org/hco/5/GRCh38#111111628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32986357-A-C

111111700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32986392-G-A

111111700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32986392-G-T

111112174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32986751-C-T

111112241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32986822-T-G

111112256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32986840-T-C

111112256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32986840-T-G

http://identifiers.org/hco/5/GRCh38#111112544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32987138-C-A

111112561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32987145-A-G

111113013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32987804-T-C

111113032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32987814-A-G

111113032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32987814-A-T

111113076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 32987835-T-C

111113076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 32987835-T-G

111113312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988026-T-G

111113408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988120-G-A

111113419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988131-A-G

111113512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988220-A-G

111113535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988243-C-T

111114420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988374-G-C

111114564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988514-A-G

111114595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32988545-T-A

111115350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32989079-C-G

111116892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32990541-T-G

111117010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32990638-T-C

111117129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32990756-A-G

111117189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32990810-C-T

111117250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32990844-G-A

111117394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32990987-C-T

111117651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991193-G-C

111117694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991237-G-A

111117770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991329-C-T

111117871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991524-G-T

111117875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991528-G-T

111117881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991545-G-A

111117911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991590-A-T

111118011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991778-A-G

111118061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991830-G-A

111118103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991872-G-A

111118692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991959-T-C

111118692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32991959-T-G

111118825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992076-T-C

http://identifiers.org/hco/5/GRCh38#111119132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32992391-C-A

111119132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992391-C-G

111119159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992425-G-A

111119159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992425-G-T

111119167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992433-T-C

111119203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992469-G-C

111119203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992469-G-T

111119223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992483-A-G

111119223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992483-A-T

111119247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992499-G-A

111119247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32992499-G-C

111119741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993005-A-G

111119741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993005-A-T

111120001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993259-G-T

111120242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993509-T-C

111120242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993509-T-G

111120299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993562-C-G

111120409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993971-C-T

111120418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32993980-A-G

http://identifiers.org/hco/5/GRCh38#111120746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32994317-A-C

111120865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994420-A-G

111120865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994420-A-T

111120874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994429-A-T

111120906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994462-A-G

http://identifiers.org/hco/5/GRCh38#111120935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32994491-A-C

111120935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994491-A-G

111120971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994518-G-A

111120980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994539-G-A

111121007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: missense variant
orthologous variants: 32994566-T-G

111121149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32994709-T-C

111121157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994717-C-G

111121157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994717-C-T

111121297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994870-A-G

111121364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32994925-G-A

111121531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995080-C-T

111121536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995085-A-G

111123219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995526-T-C

111123314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995611-G-T

111123370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995668-A-G

111123375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995673-C-G

111123622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995794-G-A

111123664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995835-T-C

111123701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995872-C-T

111123704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995875-T-C

111123722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995892-G-A

111123722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995892-G-C

111123722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32995892-G-T

111123900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: synonymous variant
orthologous variants: 32996073-T-C

111123956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32996124-T-C

111123965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32996133-G-A

http://identifiers.org/hco/5/GRCh38#111124082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32996208-A-C

111124524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32996610-T-C

111124548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32996632-G-A

111124915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997122-A-G

111124950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997151-A-G

111124980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997176-C-T

111125014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997212-G-C

111125056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997254-A-G

111125516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997624-A-T

111125568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997669-G-T

http://identifiers.org/hco/5/GRCh38#111125594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32997688-A-C

111125639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32997737-A-G

111125678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32997776-T-G

111125687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32997785-T-C

111125732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32997830-G-A

111125733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32997831-A-T

http://identifiers.org/hco/5/GRCh38#111125783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32997881-A-C

111125783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32997881-A-G

111125825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997910-G-A

111125840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32997925-G-T

111126010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32998027-A-G

111126378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32998398-G-A

111126396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32998464-G-A

http://identifiers.org/hco/5/GRCh38#111126403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32998491-A-C

111126700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: intron variant
orthologous variants: 32998863-C-T

http://identifiers.org/hco/5/GRCh38#111127344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32999360-C-A

111127344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999360-C-T

111127413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999424-T-A

111127413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999424-T-C

http://identifiers.org/hco/5/GRCh38#111127437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32999453-A-C

http://identifiers.org/hco/5/GRCh38#111127444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32999464-C-A

111127444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999464-C-G

111127444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999464-C-T

111127554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999577-G-A

111127554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999577-G-T

111127651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 32999669-G-T

http://identifiers.org/hco/5/GRCh38#111127737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32999732-C-A

111128169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33000164-G-A

111128230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33000220-G-A

111128413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33000453-A-G

111128746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33000743-A-G

http://identifiers.org/hco/5/GRCh38#111128820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33000829-C-A

111129133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33001170-G-A

111129337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33001429-G-A

http://identifiers.org/hco/5/GRCh38#111129468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33001565-C-A

111129479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33001577-A-G

111129479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33001577-A-T

111129749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33001973-A-G

111129766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33001990-A-G

111129773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33001997-G-A

111129826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33002049-T-C

111129898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33002125-C-G

111129898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33002125-C-T

111130041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30696
most severe consequence: 3 prime UTR variant
orthologous variants: 33002261-C-T