119153463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: 68664480-G-A

http://identifiers.org/hco/9/GRCh38#119153533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68664550-C-A

119153533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: 68664550-C-G

119153665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: 68664683-G-C

119153763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: 68664812-G-T

119153765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: 68664814-A-G

119153766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: 68664815-G-T

119153786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: 68664829-G-T

http://identifiers.org/hco/9/GRCh38#119153807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68664850-C-A

119153907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664931-A-T

http://identifiers.org/hco/9/GRCh38#119153919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68664943-C-A

119153919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664943-C-T

119153935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664959-T-G

119154460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665841-G-C

119154539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665931-T-A

119154540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665932-T-C

119154577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665955-G-A

119154608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665988-A-G

119155371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68667254-G-T

119156443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68669871-A-G

http://identifiers.org/hco/9/GRCh38#119156584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68670016-C-A

http://identifiers.org/hco/9/GRCh38#119156839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68670194-C-A

http://identifiers.org/hco/9/GRCh38#119157450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68670454-C-A

119157472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68670474-G-C

119157745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68670734-C-G

119158240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68670920-G-T

119158426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68672098-C-G

119158579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68672239-G-A

119158595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68672256-A-G

http://identifiers.org/hco/9/GRCh38#119158761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68672388-C-A

119159118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68672953-T-C

119159141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68672975-C-T

119159279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68673105-T-G

http://identifiers.org/hco/9/GRCh38#119159446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68673259-A-C

http://identifiers.org/hco/9/GRCh38#119159554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68673367-C-A

http://identifiers.org/hco/9/GRCh38#119159616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68673424-C-A

119159668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68673476-C-T

119159886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68673691-C-T

119159893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68673698-T-C

119159991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68673750-G-A

119160177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68673908-G-T

119160633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68674342-G-A

119160669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68674375-T-C

119160894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68674599-G-A

119161025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68674729-G-A

119161249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68674931-A-G

119161373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675049-C-T

119161404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675058-C-T

119161408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675062-T-A

119161442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675097-T-A

119162154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675340-G-A

http://identifiers.org/hco/9/GRCh38#119162182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68675368-A-C

119162337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675469-A-G

119162566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675693-C-T

119162702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68675893-G-T

119162907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68676058-A-G

http://identifiers.org/hco/9/GRCh38#119162909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68676060-A-C

119162948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68676098-C-T

119162981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68676129-G-A

119163309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68676443-A-G

119163535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68676674-A-G

119163819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68676949-A-T

119163948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68677082-G-C

http://identifiers.org/hco/9/GRCh38#119164026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68677162-C-A

119164198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68677324-G-A

119164395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68677517-C-T

119164429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68677548-A-G

119164564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68677691-G-A

http://identifiers.org/hco/9/GRCh38#119164698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68677983-C-A

119164821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678173-A-G

119164831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678179-T-A

119164979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678320-C-G

119164985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678326-G-T

119165006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678347-T-C

http://identifiers.org/hco/9/GRCh38#119165389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68678660-A-C

119165404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678670-G-A

119165600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678815-A-G

119165614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678823-C-T

119165648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678857-A-G

119165668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678877-A-G

119165672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68678881-T-C

http://identifiers.org/hco/9/GRCh38#119165860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68679008-C-A

119166181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68679314-C-T

119166235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68679365-A-G

119166251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68679382-T-C

119166306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68679437-G-T

119166462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68679585-C-T

119166534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68679657-A-G

119166554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68679687-A-T

119166663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68679779-T-A

119167004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68680123-T-G

119167114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68680276-C-G

http://identifiers.org/hco/9/GRCh38#119167180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68680342-C-A

119167396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68680558-A-G

119167405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68680567-C-G

119167423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68680585-G-A

119167447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68680609-C-T

119167459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68680621-G-A

119167488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68680647-G-C

119167678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68680837-G-A

119167825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68680984-G-A

119167825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68680984-G-C

http://identifiers.org/hco/9/GRCh38#119168194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68681353-C-A

119168194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68681353-C-G

119168194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68681353-C-T

119168258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681410-T-C

119168274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681426-G-A

119168274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681426-G-C

119168274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681426-G-T

119168284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681435-G-A

119168284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681435-G-T

119168368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681689-A-G

119168445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681786-A-G

119168498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681835-G-A

119168535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681875-C-T

119168559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681898-G-C

119168559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681898-G-T

http://identifiers.org/hco/9/GRCh38#119168580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68681919-C-A

119168583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681922-C-G

http://identifiers.org/hco/9/GRCh38#119168655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68682070-A-C

119168697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682122-A-G

119168766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682201-T-C

119168787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682222-C-T

119175613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682339-A-G

119175700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682426-G-A

119175700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682426-G-C

119175788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682513-C-T

119175829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682556-T-C

119176058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682792-C-T

119176127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682864-T-C

119176371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683112-C-T

119176442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683180-C-T

119176557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683325-T-C

119176623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683389-G-C

119176753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683526-C-G

119176753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683526-C-T

119176802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683566-T-C

119176945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683705-C-T

http://identifiers.org/hco/9/GRCh38#119177133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68683903-A-C

119177246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684032-C-G

119177270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684056-G-C

119177274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684060-G-C

119177838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684624-G-T

119177952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684739-G-C

119177957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684744-C-T

119178173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684916-T-C

119178561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685323-G-A

119178619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685377-G-T

119178983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685685-C-T

http://identifiers.org/hco/9/GRCh38#119179113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68685815-A-C

119179307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685991-G-A

http://identifiers.org/hco/9/GRCh38#119179565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68686302-A-C

http://identifiers.org/hco/9/GRCh38#119179566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68686303-A-C

119179665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686397-C-T

http://identifiers.org/hco/9/GRCh38#119179866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68686594-A-C

119179915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686643-C-G

119179925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686653-C-G

119179961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686690-C-T

119180175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686911-G-T

119180204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686940-C-T

119180231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686967-G-A

119180819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68687647-G-A

119180859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68687686-G-C

119180908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68687737-G-T

119181084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68687913-G-A

119181084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68687913-G-T

119181126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68687954-G-A

119181346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688148-G-A

119181542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688740-C-T

119181714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688888-C-T

119181756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688930-A-G

http://identifiers.org/hco/9/GRCh38#119181768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68688942-C-A

119181921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689095-T-A

119182320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689472-T-G

119182439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689618-A-G

119182441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689620-G-C

119182511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689683-A-T

119182764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689907-A-T

119183111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68690251-G-T

119183112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68690252-T-C

119183133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68690273-G-A

119183169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68690308-C-T

http://identifiers.org/hco/9/GRCh38#119183318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68690506-C-A

119183360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68690541-A-G

119183599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691349-G-T

119184073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691860-C-T

119184081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691868-A-G

119184081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691868-A-T

119184586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68692372-T-C

119184588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68692374-C-T

119184884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68692751-T-A

119185013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68692880-A-G

119185019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68692886-A-G

http://identifiers.org/hco/9/GRCh38#119185200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68693052-C-A

119185200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693052-C-T

119193834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693412-C-G

119193838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693416-G-C

119193939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693517-C-T

http://identifiers.org/hco/9/GRCh38#119193970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68693548-C-A

119194010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693587-G-A

119194046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693623-G-A

119194058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693635-G-T

119194193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693767-T-C

119194221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693793-T-C

http://identifiers.org/hco/9/GRCh38#119194276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68693848-A-C

119194437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694014-T-C

119194437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694014-T-G

119194513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694183-A-G

119194699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694334-G-A

119194845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694463-A-G

119194988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694621-T-C

http://identifiers.org/hco/9/GRCh38#119195025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68694656-C-A

119195189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694756-C-G

119195314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694892-T-A

119195367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68694946-G-A

119195429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695004-G-A

119195506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695077-C-G

119195534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695106-T-C

119195534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695106-T-G

119195640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695212-A-T

119195755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695325-G-T

http://identifiers.org/hco/9/GRCh38#119195828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68695398-C-A

119196082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695603-G-A

119196089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695610-C-T

http://identifiers.org/hco/9/GRCh38#119196245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68695930-C-A

119196245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695930-C-T

119196297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68695979-T-G

119196502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68696168-C-T

119196636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68696292-A-G

119196673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68696345-C-T

119198030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697891-A-G

119198099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697960-T-C

119198297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698183-G-A

119198404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698292-T-C

119198463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698328-C-T

119198549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698402-T-C

119198598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698451-A-G

119199002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698766-T-G

119199168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698918-C-T

119199218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698969-A-G

119199600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68699350-C-T

119199635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68699387-C-T

119199838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68699727-G-A

119199838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68699727-G-T

119199844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68699733-G-T

119200124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700001-A-T

119200161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700031-C-G

119200161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700031-C-T

119200701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700199-T-G

119200838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700333-T-C

119200866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700361-C-T

119201055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700492-C-T

119201056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68700493-C-G

119201765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68701106-C-T

119201801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68701142-G-T

119201824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68701165-G-A

119203916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68705856-T-A

119203924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68705864-C-T

119203989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68705915-A-G

119204128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706054-C-T

119204239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706167-C-T

119204347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706261-C-T

119204360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706274-G-A

119204412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706319-T-C

119204412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706319-T-G

119204439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706342-A-G

119204452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706355-G-A

119204726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706581-T-C

119204854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706709-G-A

119204932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706776-A-T

119205458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707267-T-G

119205493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707303-T-G

119205505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707315-G-A

119205544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707354-A-G

119205548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707358-C-T

119205551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707361-A-G

119205681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707487-G-A

119205704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707508-C-T

119206457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708071-T-A

119206457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708071-T-G

119206574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708165-A-G

119206592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708183-C-G

119206775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708381-T-G

119207014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708628-G-A

http://identifiers.org/hco/9/GRCh38#119207066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68708680-C-A

119207170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708774-T-G

119207224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708825-G-A

119207260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708856-G-A

119207260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708856-G-C

119207338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68708931-A-T

119207556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68709040-C-G

119207727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68709203-T-C

119208599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68710929-G-T

119208604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68710934-G-A

119208604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68710934-G-C

119208604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68710934-G-T

119208784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68711127-G-A

119208946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 68711289-T-G

119208958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68711301-G-A

119208958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68711301-G-T

119211698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68714802-G-A

119211706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68714810-G-A

119211963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68715042-C-G

119211963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68715042-C-T

119212754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68715785-T-C

119213038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68716044-C-T

119213063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68716067-G-A

119213063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68716067-G-T

119213109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68716095-T-A

119213481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68716484-C-T

119213834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68716850-A-G

119213998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: synonymous variant
orthologous variants: 68717004-C-T

119214053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: missense variant
orthologous variants: 68717059-C-T

119214339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68717333-C-T

http://identifiers.org/hco/9/GRCh38#119214359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68717353-A-C

119214360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68717354-G-A

119214465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68717459-C-G

119214493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68717487-T-C

http://identifiers.org/hco/9/GRCh38#119214560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68717559-C-A

http://identifiers.org/hco/9/GRCh38#119214577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68717574-C-A

119215041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68718184-G-A

119215476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68718598-G-A

119215569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68718694-C-T

119215636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68718772-T-C

119215726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68718875-T-G

119215897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68719128-G-T

119215913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68719201-C-T

119216348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68719748-A-G

119216398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68719798-G-A

119216460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68719861-C-T

119217055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68720431-C-T

119217348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68720744-C-T

119217740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68721177-T-A

http://identifiers.org/hco/9/GRCh38#119217783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68721230-C-A

http://identifiers.org/hco/9/GRCh38#119217941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68721393-A-C

119218055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68721502-G-A

119219929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68722831-T-C

119220040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68722942-G-A

http://identifiers.org/hco/9/GRCh38#119220541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68723440-A-C

119220636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68723540-C-T

119220726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68723632-T-C

119220890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724387-G-A

119220944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724457-T-A

119221048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724561-A-T

119221086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724599-G-A

119221179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724688-C-T

119221233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724743-C-G

119221249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724759-T-G

119221341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68724851-T-G

119221526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68725036-C-T

119221647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68725158-A-G

119221738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68725253-G-A

119221738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68725253-G-C

119222116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68725666-G-A

119222319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68725871-A-G

119222715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68726227-G-A

http://identifiers.org/hco/9/GRCh38#119222827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68726329-C-A

119222975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68726481-T-A

119223260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68726716-T-C

119223307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68726764-T-C

119223360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68726839-G-C

119223557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68727055-C-T

http://identifiers.org/hco/9/GRCh38#119223664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68727159-A-C

119224166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68727656-T-C

119224225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68727709-T-C

119224231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68727715-C-T

119224453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68727966-G-C

119224857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68728332-A-G

119224998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68728464-T-G

119225037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68728503-T-C

http://identifiers.org/hco/9/GRCh38#119225133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68728594-A-C

http://identifiers.org/hco/9/GRCh38#119225202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68728657-C-A

119225246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68728697-A-G

119226318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68733646-A-G

119226398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68733726-G-A

119226609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734155-C-T

119226632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734177-T-G

119226654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734200-T-C

119227001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734534-G-C

119227040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734573-T-C

119227067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734600-A-G

119227533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734950-C-T

119227585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68734990-T-C

119227626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68735032-A-G

119229261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68736366-A-G

119229405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68736425-C-T

119229627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68736621-G-A

119231784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739013-C-G

119231789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739018-T-C

119231874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739099-C-T

119232101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739291-T-C

119232117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739310-C-T

http://identifiers.org/hco/9/GRCh38#119232252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68739446-A-C

119232253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739447-C-T

119232282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739470-A-G

119232303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739491-A-G

119232412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739597-T-C

119232412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739597-T-G

119232507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739688-T-C

119232543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68739734-T-G

http://identifiers.org/hco/9/GRCh38#119232644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68739839-C-A

119232872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68740065-G-T

119233285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68740514-C-G

119233288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68740517-G-A

http://identifiers.org/hco/9/GRCh38#119233301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68740530-C-A

119233323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68740551-G-A

119233640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68740855-A-G

119233716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68740929-C-T

119233868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741077-C-T

119233956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741168-T-C

119234001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741213-A-G

119234082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741282-T-C

119234314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741535-T-G

119234463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741683-T-G

119234608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741791-G-T

119234617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68741799-T-A

http://identifiers.org/hco/9/GRCh38#119234971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68742079-A-C

119234989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68742100-T-C

119234989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68742100-T-G

119235213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68742262-T-C

119235753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68742777-A-G

119236422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743242-A-G

119236631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743449-G-C

119236673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743491-C-G

119236892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743665-G-C

119236928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743708-G-A

119236984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743763-A-G

119236984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743763-A-T

119237151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68743914-A-G

119238579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68744979-T-A

119238642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68745040-A-G

119238771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68745169-T-C

119238771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68745169-T-G

119239386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68745438-A-G

119239654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68745657-C-G

119239654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68745657-C-T

119240532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68746471-C-T

119241027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68746925-T-C

119241346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747244-T-A

119241834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747327-G-A

119241914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747402-A-T

119241985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747468-T-C

http://identifiers.org/hco/9/GRCh38#119242030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68747506-C-A

119242030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747506-C-G

119242030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747506-C-T

119242250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747723-G-A

119242250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747723-G-T

119242294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747769-A-G

119242358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68747830-A-G

119242582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68748018-C-T

119242594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68748030-C-T

119242635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68748071-C-T

119244731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68755825-G-A

119245194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68756310-T-C

http://identifiers.org/hco/9/GRCh38#119245433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68756476-C-A

119245640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68756676-T-C

119245687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68756723-G-C

119246124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68757160-T-G

119246637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68757212-G-A

119246817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68757365-T-A

119246839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68757387-C-G

119247082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68757630-C-G

http://identifiers.org/hco/9/GRCh38#119247223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68757763-A-C

119247353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68757892-G-C

119247967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68758516-G-T

119248107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68758629-G-A

119248749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68759249-C-T

119248814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68759312-T-C

119248822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68759320-A-T

http://identifiers.org/hco/9/GRCh38#119248898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68759396-C-A

119248898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68759396-C-T

119248940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68759434-C-T

119249090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: missense variant
orthologous variants: 68759584-A-T

119249201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68759694-A-G

http://identifiers.org/hco/9/GRCh38#119249367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68760042-A-C

119249399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760071-G-A

119249720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760366-G-A

119249801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760447-C-G

119250204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760543-C-G

119250336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760671-T-C

119250419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760754-G-A

119250453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760801-G-C

119250588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760935-T-C

119250624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68760975-C-T

119250680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68761023-G-A

119250690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68761034-G-A

119250780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68761125-C-T

119250787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68761132-C-T

http://identifiers.org/hco/9/GRCh38#119250904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68761251-C-A

119250906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68761253-A-G

http://identifiers.org/hco/9/GRCh38#119251024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68761385-C-A

119251118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68761481-A-G

119251371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68761695-G-A

119252495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68762334-T-C

119252976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68762733-T-C

119254212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764272-G-A

119254490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764478-G-A

119254542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764550-T-C

119254543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764551-A-G

119254593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764599-C-T

119254766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764857-A-G

119254815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764912-G-A

119254850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764947-G-A

119254850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68764947-G-C

http://identifiers.org/hco/9/GRCh38#119254892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68764995-C-A

119255530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68765617-G-C

http://identifiers.org/hco/9/GRCh38#119255662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68765778-A-C

119256115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68765890-C-G

119256192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68765964-C-T

119256224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68766013-A-G

http://identifiers.org/hco/9/GRCh38#119256249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68766044-A-C

119256344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68766135-C-T

119256355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68766144-T-A

119257064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68767406-C-T

119257846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768165-T-C

http://identifiers.org/hco/9/GRCh38#119257849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68768168-C-A

119257849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768168-C-T

119258132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768449-T-C

119258231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768730-T-C

119258231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768730-T-G

119258259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768755-G-A

119258297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768792-T-C

119258305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68768800-C-T

http://identifiers.org/hco/9/GRCh38#119258445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68768934-C-A

http://identifiers.org/hco/9/GRCh38#119258809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68769308-C-A

119258809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68769308-C-T

119259667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68770485-A-T

119259876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68770695-T-G

119260018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68770836-A-G

119260399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68771251-G-A

119260585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68771427-T-G

119260631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68771477-T-C

119260646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68772694-C-G

119260656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68772704-T-A

119260693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68772738-C-T

119260749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68772804-G-T

119260840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68772891-C-G

119260856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68772907-G-A

119260973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773003-C-T

http://identifiers.org/hco/9/GRCh38#119260991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68773021-A-C

119260994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773024-G-A

119261010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773034-T-G

119261206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773195-G-A

119261275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773260-A-G

119261309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773290-A-G

http://identifiers.org/hco/9/GRCh38#119261328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68773306-C-A

119261559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773520-A-G

119261598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773567-T-G

119261640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773611-G-A

119261799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773717-T-C

119261897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68773780-T-A

http://identifiers.org/hco/9/GRCh38#119262018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68773876-C-A

119262291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774142-T-G

119262329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774176-A-G

119262684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774211-A-G

119262731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774258-A-G

119262956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774480-G-T

119262971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774494-C-G

119262971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774494-C-T

119263045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774533-C-T

119263063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774551-G-A

119263063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774551-G-C

119263063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774551-G-T

119263129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774617-G-C

119263469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68774924-C-T

http://identifiers.org/hco/9/GRCh38#119263598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68775018-A-C

119263598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775018-A-T

119263637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775048-T-C

119263711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775068-C-T

119263715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775072-C-T

119263779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775086-T-C

119263780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775087-T-C

119263843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775115-T-C

119263856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775116-C-T

119263860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775120-G-A

119263898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775149-G-A

119263940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775191-C-T

119263941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775192-G-A

119263941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775192-G-T

119264216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775464-C-G

119264216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775464-C-T

119264255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68775503-C-G

119270969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68781235-A-G

119271403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68781667-T-C

119271515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68781755-T-C

119271628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68781859-C-T

119273912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783325-T-C

119274022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783438-A-T

http://identifiers.org/hco/9/GRCh38#119274070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68783486-A-C

119274114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783529-C-T

119274267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783674-G-A

119274267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783674-G-T

119274454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783860-C-T

119274469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783874-A-T

119274476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68783881-T-C

119274719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784073-C-T

119274807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784154-G-C

http://identifiers.org/hco/9/GRCh38#119274841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68784208-A-C

119274841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784208-A-G

119274848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784216-G-A

119274848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784216-G-T

119274883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784259-T-G

119274931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784317-G-A

119275805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784838-T-C

http://identifiers.org/hco/9/GRCh38#119275921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68784939-C-A

119275921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68784939-C-G

119276002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68785021-T-C

119276022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68785039-G-T

119276027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68785044-C-T

119276513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68785522-T-G

119276560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68785563-C-T

119276997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68785982-C-T

119277376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68786373-T-C

119277846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68787044-T-C

119278123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68787465-C-T

119278276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68787591-T-C

119278298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68787613-G-A

http://identifiers.org/hco/9/GRCh38#119278685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68787884-C-A

119278685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68787884-C-G

http://identifiers.org/hco/9/GRCh38#119278985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68787978-A-C

http://identifiers.org/hco/9/GRCh38#119279008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68788000-A-C

119279016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788008-G-T

119279040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788032-T-C

119279280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788355-C-T

119279363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788443-C-T

119279373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788453-C-T

119279419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788505-C-T

119279602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788688-C-T

119279754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788841-T-A

119279859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68788943-C-G

119280575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68789351-T-G

119280639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68789403-C-T

119280675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68789439-C-G

119280961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68789827-C-T

119281029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68789897-G-C

119281138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790005-T-C

119281278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790145-T-C

119281325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790192-G-C

119281385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790252-T-C

119281385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790252-T-G

119281541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790344-T-C

119282049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790786-T-C

119282132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790866-G-T

http://identifiers.org/hco/9/GRCh38#119282196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68790918-C-A

119282215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68790937-A-G

119282429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791111-G-T

119282632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791306-T-C

119282722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791397-A-G

119282723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791398-C-G

119282739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791414-T-C

119282804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791479-T-A

http://identifiers.org/hco/9/GRCh38#119282857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68791531-A-C

119282860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791534-A-T

119282869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791543-G-C

119282869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68791543-G-T

119283882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68792586-A-G

119283916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68792619-C-T

119283953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68792659-A-G

119283953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68792659-A-T

119283989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68792696-T-C

119284052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68792755-C-T

http://identifiers.org/hco/9/GRCh38#119284119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68792818-C-A

119284119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68792818-C-T

119284394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68793104-C-T

119284398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68793108-G-T

119284437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68793151-G-C

http://identifiers.org/hco/9/GRCh38#119284579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68793291-C-A

119285001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68793709-G-A

http://identifiers.org/hco/9/GRCh38#119285175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68793881-C-A

119285240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68793936-T-C

119285423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68794090-C-G

119285511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68794177-T-A

119285713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68794456-C-T

119285727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68794470-A-G

119285906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68794622-T-C

119286632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68794779-T-C

119286870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68794926-G-T

119287033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68795122-T-A

119287100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68795183-T-C

119287264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68795350-A-G

119287290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68795376-A-G

119287581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68795654-T-C

119287758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68795832-G-A

119288047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68795941-T-A

119288204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68796091-T-C

119288352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68796242-T-A

119288407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68796323-T-C

http://identifiers.org/hco/9/GRCh38#119289270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68796575-A-C

119289323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68796628-T-A

119289324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68796629-A-G

119289447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68796886-G-A

119290236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68799369-C-T

http://identifiers.org/hco/9/GRCh38#119290444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68799576-C-A

http://identifiers.org/hco/9/GRCh38#119290578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68799683-A-C

119290669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68799770-T-A

119290729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68799827-A-T

http://identifiers.org/hco/9/GRCh38#119291117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68800291-C-A

119291117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68800291-C-T

119291324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68800488-G-C

119291842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68800981-C-T

119291854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68800993-T-C

119292087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68801226-G-C

119292443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68802961-A-G

119292798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68803308-T-G

119292856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68803437-G-A

119292857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68803438-A-T

119292914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68803493-C-T

119293171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68804186-C-G

119293179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68804196-T-C

119293240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68804261-G-A

119293604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68804595-T-C

119293612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68804603-T-A

http://identifiers.org/hco/9/GRCh38#119293763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68804726-A-C

119297511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68805799-G-A

119297609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68805874-G-C

119297702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68805970-T-G

119297733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68806001-A-G

119297876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68806158-A-G

http://identifiers.org/hco/9/GRCh38#119297906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68806188-A-C

119297906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68806188-A-G

119297941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68806225-C-T

119298463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, undefined
orthologous variants: 68806748-G-A

http://identifiers.org/hco/9/GRCh38#119298474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68806759-C-A

119298482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, undefined
orthologous variants: 68806773-C-T

119300742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68808993-T-C

119300776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809023-C-T

119300860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809114-C-T

119301155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809392-G-T

119301216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809445-A-G

http://identifiers.org/hco/9/GRCh38#119301240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68809470-C-A

119301259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809489-A-G

119301432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809632-C-T

119301530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809686-G-A

119301530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809686-G-C

119301729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809868-A-G

119301736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68809875-A-G

http://identifiers.org/hco/9/GRCh38#119301935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68810064-C-A

119301935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68810064-C-T

119301977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68810096-G-A

119302120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68810224-G-A

119302193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68810303-C-T

http://identifiers.org/hco/9/GRCh38#119302195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68810305-C-A

119302195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68810305-C-T

http://identifiers.org/hco/9/GRCh38#119302231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68810343-C-A

119303119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68811243-A-G

119303206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68811320-C-T

http://identifiers.org/hco/9/GRCh38#119303218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68811332-C-A

119303875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68811902-C-G

119303875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68811902-C-T

119304301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68812203-G-A

119304466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68812361-A-G

119304823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68812681-C-T

119304828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68812685-T-G

119305193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68814415-G-C

http://identifiers.org/hco/9/GRCh38#119305335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68814545-C-A

119305349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68814559-G-A

119305543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68814740-G-A

119305867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68815067-G-A

119306098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68815278-G-A

119306333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68815498-G-A

119306342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68815507-G-C

http://identifiers.org/hco/9/GRCh38#119306669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68815864-A-C

119306669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68815864-A-G

119306969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68816179-A-G

119307039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68816246-C-T

119307861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68816545-T-C

119308200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68816877-A-T

119308329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68816960-T-C

119308371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68817002-G-A

119308375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68817006-G-A

119308375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68817006-G-C

119308448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68817084-A-G

119308609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68817259-T-C

119308723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68817369-A-G

119308770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68817416-G-A

http://identifiers.org/hco/9/GRCh38#119308932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68817586-A-C

http://identifiers.org/hco/9/GRCh38#119309028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68817784-C-A

119309247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818046-C-T

119309283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818070-G-A

119309377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818157-C-T

119309671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818390-C-T

119309867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818570-C-T

119310013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818624-T-C

119310106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818717-T-C

119310240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68818846-C-T

119310505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819122-G-A

119310511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819128-A-T

119310638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819234-G-A

119310643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819239-C-T

119310782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819364-G-T

http://identifiers.org/hco/9/GRCh38#119310783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68819365-C-A

119310883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819436-G-T

119311047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819569-G-C

http://identifiers.org/hco/9/GRCh38#119311062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68819584-C-A

119311302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68819830-C-T

119312589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822456-G-A

119312597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822464-C-G

http://identifiers.org/hco/9/GRCh38#119312661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68822529-A-C

119312661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822529-A-G

119312857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822706-T-C

119312895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822738-G-A

119312895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822738-G-T

119312977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822814-T-G

119313023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822861-G-A

119313023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822861-G-C

119313023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68822861-G-T

119313193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: missense variant
orthologous variants: 68823029-G-T

119313497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823315-G-A

119313497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823315-G-C

119313498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823316-A-T

119313526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823341-C-T

119313578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823380-C-T

119313613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823413-T-C

119313613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823413-T-G

119313671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823469-G-A

119314138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823930-G-A

119314138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823930-G-T

119314163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68823956-G-A

119314228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68824012-G-A

119314228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68824012-G-C

119314228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68824012-G-T

119318106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68824790-C-G

119318106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68824790-C-T

119318263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68824947-T-C

http://identifiers.org/hco/9/GRCh38#119318547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68825225-C-A

119318547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68825225-C-T

119319445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68826614-T-C

119319560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68826699-G-A

119319606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68826745-T-C

119319622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68826759-T-C

119319695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68826810-G-T

119319980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68827064-A-G

119320541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68827445-C-T

119321986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68828229-G-A

119322103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68828346-C-T

119322351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron_variant, undefined
orthologous variants: 68828593-G-A

119322677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68828887-T-C

119322917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68829091-T-C

119323405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68829550-G-C

119323594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68829739-G-C

119324189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831258-A-G

119324272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831324-C-T

119324287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831343-C-T

119324383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831449-C-T

119324388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831454-C-T

119324389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831455-C-G

119324579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831673-C-T

http://identifiers.org/hco/9/GRCh38#119324611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68831710-A-C

119324611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831710-A-G

119324636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831738-A-G

119324821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831890-C-G

119324821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68831890-C-T

119325299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68832279-A-T

119325423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68832380-T-C

http://identifiers.org/hco/9/GRCh38#119325499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68832454-C-A

http://identifiers.org/hco/9/GRCh38#119325749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68832598-C-A

119325774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68832624-G-T

119325884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68832689-A-G

119326700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68833555-G-A

119326914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68833747-G-A

119326914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68833747-G-C

119327446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68833969-C-T

119327455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68833978-T-A

119327455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68833978-T-C

119327551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834069-T-A

119327588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834112-A-T

119327624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834153-G-C

119327652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834219-G-A

119327718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834377-A-T

119327740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834399-G-C

119327740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834399-G-T

119328350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834895-G-A

119328350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834895-G-C

119328390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834920-C-G

119328415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68834950-T-A

119328544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68835086-G-T

119328816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68835362-C-T

119328849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68835382-G-T

http://identifiers.org/hco/9/GRCh38#119328956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68835486-C-A

119329033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68835585-G-A

119329090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68835636-G-A

119329103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68835649-C-T

http://identifiers.org/hco/9/GRCh38#119333925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68837109-A-C

119334015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68837200-A-G

119334062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68837239-T-C

119334162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68837332-T-C

119334282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68837452-A-G

119334869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68838523-C-T

119335696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68839891-G-A

119335905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840103-T-C

119335935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840133-C-T

http://identifiers.org/hco/9/GRCh38#119336243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68840436-C-A

119336263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840456-G-A

119336264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840457-G-A

119336350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840535-G-A

119336350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840535-G-C

119336422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840656-C-G

119336691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840916-G-A

119336698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840923-C-G

119336698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840923-C-T

119336766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68840989-G-A

119336794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841017-G-A

119336807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841029-T-A

119336818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841040-G-T

119337038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841243-C-T

119337046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841249-G-A

119337220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841428-C-G

119337342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841551-G-C

119337364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841571-C-T

119337631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68841870-C-T

119337786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842020-C-T

119338375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842357-A-T

119338548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842533-T-G

119338691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842557-T-A

119338691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842557-T-C

119338691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842557-T-G

http://identifiers.org/hco/9/GRCh38#119338952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68842756-A-C

119339137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842843-G-A

119339137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842843-G-C

119339137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842843-G-T

119339138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842844-G-C

119339198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68842903-C-T

119339319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68843022-C-T

119339329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68843032-G-A

119339344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68843047-G-C

119339620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68843860-C-T

119340074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844182-G-A

http://identifiers.org/hco/9/GRCh38#119340118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68844225-A-C

119340262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844368-A-G

119340309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844415-G-C

119340359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844465-G-T

http://identifiers.org/hco/9/GRCh38#119340404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68844510-C-A

119340407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844513-C-G

119340409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844515-G-A

119340424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844526-G-A

http://identifiers.org/hco/9/GRCh38#119340478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68844583-C-A

119340580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68844678-T-A

119342336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68845849-A-G

119342343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68845856-A-G

http://identifiers.org/hco/9/GRCh38#119342399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68845912-C-A

119342409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68845922-G-T

119342977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68846544-T-C

119343020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68846585-G-A

119343149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68846710-G-T

119343166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68846727-G-A

119343234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68846796-C-T

http://identifiers.org/hco/9/GRCh38#119343407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68846969-C-A

119343586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68847116-C-T

119343676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68847206-C-T

119344668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68848011-T-C

119344819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68848173-G-A

119344819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68848173-G-C

http://identifiers.org/hco/9/GRCh38#119344861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68848283-C-A

119344915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68848333-G-C

119345108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68848517-C-T

http://identifiers.org/hco/9/GRCh38#119345213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68848628-C-A

119345565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68848967-T-C

119345668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68849017-G-T

119345786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68849060-T-C

119345875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68849147-T-C

119346126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68849360-C-G

http://identifiers.org/hco/9/GRCh38#119346179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68849397-A-C

119346222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68849445-G-A

119346266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68849486-A-T

119347025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850183-G-T

119347053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850211-C-T

119347194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850342-T-G

119347423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850530-T-C

119347660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850736-C-T

119347678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850754-T-A

119347717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850793-C-T

119347809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850893-T-C

119347846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68850926-C-T

119348002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68851107-G-A

119348322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68851404-T-C

http://identifiers.org/hco/9/GRCh38#119348834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68851841-C-A

119348986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68851990-T-C

119349146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852156-C-T

119349156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852190-C-T

119349202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852313-G-A

119349210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852324-G-C

119349322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852606-A-T

119349390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852760-T-G

http://identifiers.org/hco/9/GRCh38#119349521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68852891-C-A

119349521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852891-C-T

119349591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68852961-G-A

119349791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853168-G-T

119349941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853297-T-G

119349977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853338-T-C

119350153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853496-G-A

119350167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853507-C-T

119350281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853618-T-C

119350579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853949-T-G

119350614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68853984-A-G

http://identifiers.org/hco/9/GRCh38#119350664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68854046-A-C

119350695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68854089-C-G

119350695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68854089-C-T

119350717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68854110-T-C

119351540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68855441-G-A

119351701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68855606-T-G

http://identifiers.org/hco/9/GRCh38#119352145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68855713-C-A

119352145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68855713-C-T

119352241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68855811-G-A

119352257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68855827-C-T

119352295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68855862-C-T

119352339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68855909-T-C

119352929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68856269-G-T

119352957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68856294-C-G

119353033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68856937-C-T

119353058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68856962-A-G

119353379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68857257-C-T

119353538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68857395-C-T

119353592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68857451-A-G

119353955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68857766-G-A

119354174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68858614-T-C

http://identifiers.org/hco/9/GRCh38#119355258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68860595-C-A

119355258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68860595-C-G

119355258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68860595-C-T

119355315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68860653-G-A

http://identifiers.org/hco/9/GRCh38#119355348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68860686-C-A

119355348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68860686-C-T

119355382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68860720-T-C

119355956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68860966-C-T

119356009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68860982-A-T

119356045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68861013-T-C

119356059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68861027-A-G

http://identifiers.org/hco/9/GRCh38#119356089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68861049-C-A

119356184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68861226-G-A

119357234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68862413-T-C

119357294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68862472-A-T

http://identifiers.org/hco/9/GRCh38#119357509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68862700-A-C

119357572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68862768-T-C

119357582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68862778-C-T

119357673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68862873-G-A

119357673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68862873-G-T

119357800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68862992-C-G

119357941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863159-G-T

http://identifiers.org/hco/9/GRCh38#119358065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68863269-A-C

119358132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863339-T-C

119358292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863494-T-C

119358292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863494-T-G

119358354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863564-T-A

119358373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863584-G-A

119358373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863584-G-T

119358702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863614-A-G

119358708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863620-A-T

119358758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863659-T-C

119358975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68863868-G-A

119359568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68864139-G-A

119359571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68864142-T-A

119359662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68864231-A-G

http://identifiers.org/hco/9/GRCh38#119359860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68864421-C-A

119359935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68864494-C-G

119359935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68864494-C-T

http://identifiers.org/hco/9/GRCh38#119360009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68864630-C-A

119360009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68864630-C-T

119360407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68865055-T-C

119360407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68865055-T-G

119360518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68865162-G-A

119360851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68865474-T-C

119361000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68865625-C-T

119362134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866216-G-C

119362372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866451-T-A

119362393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866472-C-T

119362401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866480-T-C

http://identifiers.org/hco/9/GRCh38#119362576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68866646-C-A

119362576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866646-C-T

119362611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866681-C-T

119362720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866775-C-T

119362846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68866884-C-T

119363552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68867296-C-T

119363663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68867405-G-A

119363927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68867622-C-G

119365132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68868297-G-C

119365245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68868407-T-G

119365535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68868675-T-C

119365612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68868747-T-C

119365717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68868870-C-G

119365809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68868963-G-C

119365890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869054-T-C

119365939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869103-A-G

119366202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869367-T-A

119366508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869763-G-A

119366508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869763-G-C

119366516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869771-G-A

119366516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869771-G-C

119366520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869775-G-A

119366528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869783-G-A

119366536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869791-G-A

119366544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869832-G-C

119366553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869841-T-C

119366554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869842-G-C

119366554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68869842-G-T

119366814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870102-G-A

119366917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870195-G-A

119367127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870410-C-G

119367249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870493-T-A

119367249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870493-T-G

119367250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870494-A-T

119367513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870722-G-A

119367605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870814-T-C

119367605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870814-T-G

119367759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870965-T-A

119367771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870977-T-C

119367771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68870977-T-G

119367994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: intron variant
orthologous variants: 68871187-A-G

http://identifiers.org/hco/9/GRCh38#119369297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#68872491-C-A

119369297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: 5 prime UTR variant
orthologous variants: 68872491-C-T

119369406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2687
most severe consequence: 5 prime UTR variant
orthologous variants: 68872577-T-C