57376094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679195-G-A

57376094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679195-G-T

57376111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679178-G-T

57376127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679170-G-A

57376127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679170-G-T

57376147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679153-G-A

57376147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679153-G-T

http://identifiers.org/hco/15/GRCh38#57376149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71679151-C-A

57376149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679151-C-T

57376184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679118-A-G

57376263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: non coding transcript exon variant
orthologous variants: 71679075-G-T

http://identifiers.org/hco/15/GRCh38#57376295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71679049-C-A

57376295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679049-C-T

57376381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71678969-C-T

57376412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71678932-C-T

57376414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71678930-G-A

57376483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71678867-T-C

57376523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678827-G-A

57376523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678827-G-T

57376546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71678804-G-A

http://identifiers.org/hco/15/GRCh38#57376590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71678766-C-A

57376590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678766-C-G

57376590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678766-C-T

57376623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678732-G-A

57376623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678732-G-C

57376623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678732-G-T

57376649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678724-G-A

57376649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678724-G-T

http://identifiers.org/hco/15/GRCh38#57376683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#71678688-C-A

57376683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71678688-C-T

http://identifiers.org/hco/15/GRCh38#57376809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71678570-C-A

57376809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71678570-C-T

57376932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678533-G-A

57376996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678469-G-T

57376997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678468-A-G

http://identifiers.org/hco/15/GRCh38#57377032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#71678438-C-A

http://identifiers.org/hco/15/GRCh38#57377038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71678430-C-A

57377038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678430-C-G

http://identifiers.org/hco/15/GRCh38#57377089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71678382-C-A

57377089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678382-C-G

57377089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678382-C-T

http://identifiers.org/hco/15/GRCh38#57377091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71678380-C-A

57377091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678380-C-G

57377091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678380-C-T

57377183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71678290-T-C

57377286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71678181-T-C

57377339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71678138-C-T

57377474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677976-T-C

57377598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677928-A-T

57377628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71677899-A-G

57377727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677795-G-C

57377780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677751-C-T

57377859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677697-A-T

57378088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677454-A-G

57378097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677445-A-G

57378116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677427-A-G

57378346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677201-G-A

57378346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677201-G-T

http://identifiers.org/hco/15/GRCh38#57378822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71677060-C-A

57378837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677046-G-C

57378837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677046-G-T

57378862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677021-G-C

57378862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677021-G-T

57378986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676918-G-A

http://identifiers.org/hco/15/GRCh38#57379000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71676902-C-A

57379000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676902-C-T

57379011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676891-G-C

57379093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676841-A-G

57379131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676804-G-A

57379131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676804-G-T

57379602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676378-T-C

57379755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676171-T-C

57379774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676152-G-C

57379820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676117-G-A

57380188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675799-C-T

57380210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675782-T-A

57380210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675782-T-C

57380237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675743-T-G

57380301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675696-T-C

http://identifiers.org/hco/15/GRCh38#57380607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71675378-A-C

http://identifiers.org/hco/15/GRCh38#57380853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71675117-C-A

57380853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675117-C-G

57380853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675117-C-T

57380854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675116-G-A

57380854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71675116-G-T

57381919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673942-A-G

57381975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673886-G-C

57382132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673726-C-T

57382245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673610-T-A

57382304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673552-A-G

57382345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673511-G-A

57382345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673511-G-C

57382359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673498-G-A

57382441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673429-G-A

57382506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673355-C-T

57383027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673026-G-A

57383036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71673017-G-A

57383105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672969-G-C

57383200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672899-T-C

57383235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672870-A-G

http://identifiers.org/hco/15/GRCh38#57384054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71672509-A-C

57384055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672508-A-G

57384215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672376-G-T

57384236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672349-G-T

57384331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672216-T-C

57384368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672188-A-G

57384368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672188-A-T

57384390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672166-C-T

http://identifiers.org/hco/15/GRCh38#57384409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71672147-A-C

57384421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672135-G-A

57384440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672116-C-T

57384457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672084-G-A

57384495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672020-A-T

57384517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71672001-T-C

57384530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71671988-G-T

57384531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71671986-C-G

57386006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71670993-T-C

57386230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71670773-G-A

57387085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668865-G-A

57387095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668855-T-G

57387097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668853-C-T

57387204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668754-T-G

57387494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668382-C-T

57387674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668186-C-T

57387677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668183-C-T

57387761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668099-G-A

57387789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668071-G-A

57387878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667991-C-T

57387913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667890-G-A

57387923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667877-G-A

57388119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667581-T-C

57388294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667379-A-G

57388366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667287-G-A

57392561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71666414-G-A

57392886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71666054-A-T

57393013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665906-T-C

http://identifiers.org/hco/15/GRCh38#57393120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71665803-C-A

57393120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665803-C-G

57393325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665586-T-C

57393370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665541-T-C

57393493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665450-T-C

57393530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665407-T-A

57393701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665226-A-G

57393705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665222-G-A

57393727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665186-T-G

57393747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665166-C-T

57393805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71665107-A-G

57395285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664620-C-G

57395285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664620-C-T

57395423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664446-C-T

57395428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664441-G-A

57395494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664387-G-A

57395494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664387-G-C

57395842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664054-C-T

57395848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71664048-A-G

57398189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71663355-A-T

57398278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71663301-A-G

57398466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71663116-G-T

http://identifiers.org/hco/15/GRCh38#57398514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71663068-C-A

57398514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71663068-C-T

http://identifiers.org/hco/15/GRCh38#57398580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71663009-C-A

http://identifiers.org/hco/15/GRCh38#57398647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71662937-C-A

57398650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71662934-A-G

http://identifiers.org/hco/15/GRCh38#57398727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71662846-A-C

57399396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71662478-G-A

57399463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71662427-T-G

57402719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71661913-G-A

57402719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71661913-G-T

57402722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71661910-T-C

57402733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71661899-A-G

57402744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71661886-G-A

57402744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71661886-G-T

57402764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71661870-A-G

57403108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71661530-C-T

57403371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71661268-C-T

57403584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71661057-C-T

57403623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71661023-C-T

57403708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660943-A-G

57403782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660871-C-T

57403785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660868-G-T

57403823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660830-T-C

57403900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660750-C-G

57403900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660750-C-T

57403962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660702-T-G

57404168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660505-C-G

57404168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660505-C-T

57404299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660388-T-C

57404359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660334-A-G

57404378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660292-A-G

57404425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660248-C-T

57404672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71660003-G-A

57404733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71659930-T-A

http://identifiers.org/hco/15/GRCh38#57405204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71658714-C-A

57405204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71658714-C-T

http://identifiers.org/hco/15/GRCh38#57405244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71658675-C-A

http://identifiers.org/hco/15/GRCh38#57405251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71658668-C-A

57405251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71658668-C-T

57405281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71658647-A-G

57405287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71658644-A-G

57405288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71658643-C-T

57405502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658492-A-T

57405593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658411-G-T

57405783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658289-T-C

57405803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658269-T-C

57405809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658263-T-G

57405811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658261-C-G

57405811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658261-C-T

57405815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658257-T-C

57405819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658253-T-C

57405823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658249-T-C

57405856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658218-C-T

57405861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658213-T-G

57405869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71658205-T-C

http://identifiers.org/hco/15/GRCh38#57405928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71657931-C-A

57405972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71657867-A-G

57405980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71657859-C-T

57405981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71657858-C-T

57406088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657740-A-G

57406088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657740-A-T

http://identifiers.org/hco/15/GRCh38#57406108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71657718-C-A

57406108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657718-C-T

http://identifiers.org/hco/15/GRCh38#57406109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71657717-C-A

57406110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657716-A-T

57406211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657627-G-A

57406211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657627-G-C

57406211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657627-G-T

57406265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657570-G-C

57406373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657465-A-T

57406514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657330-A-G

57406557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657288-A-G

57406627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657205-C-T

http://identifiers.org/hco/15/GRCh38#57406650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71657186-C-A

57406653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657183-G-A

57406712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71657130-T-A

57407095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71656840-G-T

57407262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71656544-A-T

57407318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71656488-C-T

57407353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71656456-A-T

http://identifiers.org/hco/15/GRCh38#57408114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71656040-A-C

57408133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71656027-A-G

57408235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655930-C-G

57408558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655591-G-C

57408596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655555-T-C

57409250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655244-G-A

57409280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655225-C-T

57409343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655170-C-T

57409382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655132-A-G

57409450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71655061-C-T

http://identifiers.org/hco/15/GRCh38#57409451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71655060-A-C

57409535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71654979-A-G

57409949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71653919-G-A

57409949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71653919-G-T

57410203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71653686-A-T

57415286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651629-G-A

57415329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651596-A-G

57415343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651582-A-G

57415397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651526-A-G

57415431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651493-T-C

57415566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651390-C-T

57415719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651283-G-T

57415927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651145-G-A

57415972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651128-C-G

http://identifiers.org/hco/15/GRCh38#57416858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71649857-A-C

57417604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649363-G-C

57417604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649363-G-T

57417606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649361-G-T

57417662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649329-C-T

57417670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649321-T-G

57417673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649318-A-T

57417788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649291-T-C

http://identifiers.org/hco/15/GRCh38#57417842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71649234-A-C

57417970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649115-G-C

57418353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648762-T-C

57418440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648678-A-T

57418442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648676-C-G

57418656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648379-C-G

57422215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71646113-A-T

57422365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645954-C-G

57422365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645954-C-T

57422697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645643-G-T

57422713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645627-T-A

57422868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645471-T-C

http://identifiers.org/hco/15/GRCh38#57423021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71645347-A-C

57423021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645347-A-G

57423021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645347-A-T

57423102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645267-T-G

57423265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645103-G-A

57426947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71643433-G-A

57427058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71643352-T-A

http://identifiers.org/hco/15/GRCh38#57427491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#71642579-C-A

57427682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71642446-T-C

57427880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71642264-A-T

57428325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641243-A-G

57428327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641241-C-T

57428760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640819-C-T

57428816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640751-A-T

57429329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639948-T-C

http://identifiers.org/hco/15/GRCh38#57429342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71639935-A-C

57429342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639935-A-G

57429487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639793-C-T

http://identifiers.org/hco/15/GRCh38#57429553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71639732-A-C

57429553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639732-A-G

57431079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637899-G-A

57431171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637802-T-C

57431223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637520-T-C

57431472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637304-A-T

57431945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636795-G-A

57431945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636795-G-C

57431957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636783-A-G

57432010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636732-C-G

57432010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636732-C-T

57432420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636386-C-G

http://identifiers.org/hco/15/GRCh38#57432445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71636362-A-C

57432615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636195-C-T

57432858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635960-A-G

57432858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635960-A-T

57437572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633703-T-G

57437782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633549-C-G

57437782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633549-C-T

57437783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633548-G-A

57437783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633548-G-C

57437783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633548-G-T

57438015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71633332-G-A

57438015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71633332-G-C

57438015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71633332-G-T

57438027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71633320-C-T

57438071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: synonymous variant
orthologous variants: 71633276-T-C

57438249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: synonymous variant
orthologous variants: 71633098-C-T

http://identifiers.org/hco/15/GRCh38#57438267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71633080-A-C

57438267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71633080-A-G

57438441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632903-C-T

57438510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632834-G-A

57438564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632780-T-G

57438741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632603-G-A

57438777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632567-C-G

57438777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632567-C-T

57438954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632390-T-A

http://identifiers.org/hco/15/GRCh38#57439137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71632207-A-C

57439137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632207-A-G

57439206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632138-T-C

57439288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71632056-T-C

57439385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: synonymous variant
orthologous variants: 71631971-C-G

57439591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71631768-C-T

57439715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71631680-G-A

57439715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71631680-G-T

http://identifiers.org/hco/15/GRCh38#57439719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71631676-C-A

http://identifiers.org/hco/15/GRCh38#57440087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71631210-A-C

57440190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71631114-C-T

http://identifiers.org/hco/15/GRCh38#57440247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71631062-C-A

57440281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71631037-G-C

57440281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71631037-G-T

http://identifiers.org/hco/15/GRCh38#57440297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71631025-C-A

57440297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71631025-C-T

57440300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71631022-A-T

57440358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71630930-A-T

57440375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: splice acceptor variant
orthologous variants: 71630910-A-G

57440829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629966-T-G

57441102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629797-A-G

57441153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629753-G-A

57441306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629643-C-T

http://identifiers.org/hco/15/GRCh38#57441840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71629361-C-A

57441840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629361-C-T

57441876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629326-A-T

57441977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629267-G-A

57441989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629255-G-C

http://identifiers.org/hco/15/GRCh38#57442248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71629084-A-C

57442295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629051-G-A

57442295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629051-G-C

57442295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629051-G-T

57442299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629047-G-A

57442299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629047-G-T

57442345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71629008-A-G

57442455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71628899-G-C

57442480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: splice donor variant
orthologous variants: 71628874-T-C

57442494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71628859-G-A

57442494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71628859-G-T

57442527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71628826-G-A

57444555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71627892-T-G

57446002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71627036-C-T

57451133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71625084-T-A

57451209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71625018-A-G

http://identifiers.org/hco/15/GRCh38#57451305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71624944-A-C

57451312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624938-G-A

57451363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624901-T-C

57451405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624867-A-G

57451423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624850-T-A

57451423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624850-T-C

57451423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624850-T-G

57451508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: synonymous variant
orthologous variants: 71624769-T-C

57451691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624542-G-A

57451691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624542-G-T

57451703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624532-T-C

http://identifiers.org/hco/15/GRCh38#57451704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71624531-C-A

57451704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624531-C-T

http://identifiers.org/hco/15/GRCh38#57451730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71624505-A-C

57451730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624505-A-G

57452057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624183-A-G

57452091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624144-T-G

http://identifiers.org/hco/15/GRCh38#57452093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71624142-C-A

57452093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624142-C-G

57452093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71624142-C-T

57452297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71623680-C-G

57452297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71623680-C-T

http://identifiers.org/hco/15/GRCh38#57452309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71623668-C-A

57452309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71623668-C-T

http://identifiers.org/hco/15/GRCh38#57452372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71623607-C-A

57452372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71623607-C-G

57452372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71623607-C-T

57452386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71623593-T-A

57452386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71623593-T-C

http://identifiers.org/hco/15/GRCh38#57452410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71623569-C-A

57452410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71623569-C-T

http://identifiers.org/hco/15/GRCh38#57452805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71623155-C-A

57453419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622943-T-C

57453476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622887-A-G

57453569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622854-G-C

http://identifiers.org/hco/15/GRCh38#57453620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71622803-C-A

57453620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622803-C-G

57453733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71622688-A-G

57453783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: stop gained
orthologous variants: 71622638-C-T

57453786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71622635-T-C

57453853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622577-G-C

http://identifiers.org/hco/15/GRCh38#57453855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71622575-C-A

57453855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622575-C-T

http://identifiers.org/hco/15/GRCh38#57453900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71622531-A-C

57453900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622531-A-G

57453900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622531-A-T

57453904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622527-A-G

http://identifiers.org/hco/15/GRCh38#57453921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71622510-C-A

57453921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71622510-C-T

http://identifiers.org/hco/15/GRCh38#57455577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71621415-C-A

57455597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71621398-C-G

57455597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71621398-C-T

57455615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71621380-C-T

57455689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71621316-A-T

http://identifiers.org/hco/15/GRCh38#57455785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71621006-A-C

http://identifiers.org/hco/15/GRCh38#57456172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71620674-A-C

57456188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71620658-A-G

57456193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71620653-A-G

57456238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71620608-G-C

57456255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71620590-C-G

57457080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71618764-A-G

57457098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71618748-T-C

57457282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71618628-G-A

57457310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71618592-C-T

57457453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71618456-G-A

57458364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71616878-C-G

57458505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71616741-C-T

57458604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71616659-A-G

http://identifiers.org/hco/15/GRCh38#57458760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71616527-A-C

57458767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71616520-C-T

57459047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71615698-G-A

57459094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71615650-T-C

57459097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71615647-T-A

57459183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71615559-G-A

57459274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71615466-T-C

57459439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71614894-G-A

http://identifiers.org/hco/15/GRCh38#57460121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71614250-A-C

57460174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71614129-A-G

57460203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71614065-A-T

57460214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71614033-G-A

57460214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71614033-G-C

57460788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71613494-A-G

http://identifiers.org/hco/15/GRCh38#57461333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71612967-C-A

57461350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612928-C-T

57461530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612788-G-A

57461530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612788-G-C

57461547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612771-G-A

57461547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612771-G-T

57461552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612767-T-G

57461604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612715-A-G

http://identifiers.org/hco/15/GRCh38#57461669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71612653-C-A

57461669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612653-C-G

57461669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612653-C-T

57461843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71612477-A-G

57461920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612397-T-A

57461920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612397-T-C

57462020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612331-A-G

57462040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612311-G-A

57462040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612311-G-T

57462053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612299-G-T

57462198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71612164-C-T

http://identifiers.org/hco/15/GRCh38#57462257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71612123-A-C

57462497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611884-G-A

57462497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611884-G-T

57462878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611539-T-G

57462948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611476-T-C

57463017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611379-C-G

57463022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611374-G-C

http://identifiers.org/hco/15/GRCh38#57463219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71611200-C-A

57463292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611129-G-T

http://identifiers.org/hco/15/GRCh38#57463297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71611124-A-C

57463297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71611124-A-G

57463687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71610769-C-T

57463868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71610631-A-T

57464109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71610399-G-T

57464242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71610272-C-T

http://identifiers.org/hco/15/GRCh38#57465314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71608899-C-A

57465314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608899-C-T

57465719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608789-T-C

57465893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608615-G-A

57465919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608589-A-G

57465935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608574-G-A

57465935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608574-G-T

57466142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608393-G-C

57466177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608362-G-A

57466286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71608260-A-G

57466598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71607633-G-A

57466817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71607296-A-T

57466859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71607255-G-A

57467152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71606720-T-A

57467415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71606460-G-A

57467480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71606404-G-T

57469876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71605620-T-C

57470421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604800-G-C

57470540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604707-A-G

57470552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604696-G-A

57470552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604696-G-T

57470569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604679-C-T

57470680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604213-C-T

57470819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604071-T-C

57470819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71604071-T-G

57471296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71603401-G-T

57471507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71603205-A-G

57471749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71602959-A-G

57471765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71602944-T-G

57471769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71602940-G-A

http://identifiers.org/hco/15/GRCh38#57472559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71601797-A-C

57472559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601797-A-T

57472561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601795-G-A

57472647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601727-T-C

57472659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601715-C-T

57472754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601640-C-G

57472754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601640-C-T

57472755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601639-A-G

57472758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601636-T-C

57472831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601569-G-A

http://identifiers.org/hco/15/GRCh38#57472992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71601309-C-A

57472992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601309-C-T

57473240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71601086-G-C

57473304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600994-C-G

57473411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600887-T-C

57473436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600862-G-A

57473436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600862-G-T

57473674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600658-A-G

http://identifiers.org/hco/15/GRCh38#57473712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71600620-A-C

57473773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600560-A-G

http://identifiers.org/hco/15/GRCh38#57473935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71600409-A-C

57473935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600409-A-T

57473949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600395-G-A

57473949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71600395-G-T

57476660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71599615-T-C

57476700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71599575-G-A

57476716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71599559-C-T

57477159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71597836-A-T

57477238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71597754-T-A

57477255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71597737-A-T

57477540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71597487-C-T

57477551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71597476-T-C

57477698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71597355-G-A

http://identifiers.org/hco/15/GRCh38#57477727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71597326-C-A

57477828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71597235-C-T

57477842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71597220-A-G

57478040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71597032-A-G

57478106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71596974-T-C

57478121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71596964-T-C

57478155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71596931-G-T

57478234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71596865-G-A

57478234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71596865-G-T

http://identifiers.org/hco/15/GRCh38#57478261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71596840-A-C

57478261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71596840-A-G

57485498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71592881-A-G

http://identifiers.org/hco/15/GRCh38#57485660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71592721-A-C

57485660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71592721-A-G

57485769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71592590-T-C

57485794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71592565-A-T

57485840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71592521-G-A

57485914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, undefined
orthologous variants: 71592463-C-T

57486019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, undefined
orthologous variants: 71592293-T-C

57486110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, undefined
orthologous variants: 71592206-C-G

57486125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, undefined
orthologous variants: 71592190-G-A

57486299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71592053-T-C

57486632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71591621-T-C

57486804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71591490-G-A

57486815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71591479-T-C

http://identifiers.org/hco/15/GRCh38#57492225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71590673-A-C

57492225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71590673-A-G

57492278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71590614-T-C

57492346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71590548-A-T

57492576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71590319-G-A

http://identifiers.org/hco/15/GRCh38#57492762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71590125-A-C

http://identifiers.org/hco/15/GRCh38#57492784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71590104-C-A

57492843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71590044-C-T

57493333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71588561-C-T

57493449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71588462-C-T

http://identifiers.org/hco/15/GRCh38#57493475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71588437-C-A

57493475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71588437-C-G

57493475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71588437-C-T

57493534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71588358-T-C

57493614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71588077-T-C

57493655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71588036-G-A

57493909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587799-C-G

57493917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587791-A-T

57493979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587753-G-C

57493980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587752-A-T

57494010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587722-C-T

57494031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587697-G-C

57494064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587662-A-G

http://identifiers.org/hco/15/GRCh38#57494132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71587559-C-A

57494132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587559-C-T

57494156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587535-C-T

57494263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587430-G-A

57494311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587389-G-T

57494347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587351-C-T

57494427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587272-C-T

57494549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587165-A-G

57494549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587165-A-T

57494579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587135-G-A

57494663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71587051-T-G

57494749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586967-G-T

57494843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586872-C-T

57494923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586792-C-T

http://identifiers.org/hco/15/GRCh38#57495117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71586616-C-A

57495196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586535-G-A

57495286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586465-C-G

57495286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586465-C-T

57495556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586209-G-C

57495669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71586091-T-A

57495863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71585036-G-A

57495866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71585033-A-G

57495866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71585033-A-T

57495869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71585030-T-C

57496036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71584867-A-T

57497247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71583432-G-A

57497263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71583383-T-C

57497344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, undefined
orthologous variants: 71583278-T-G

57497357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, undefined
orthologous variants: 71583266-T-G

57497638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71582995-C-T

57497699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71582935-G-A

57498000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71582085-A-T

57499918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71579608-G-A

57499953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71579573-C-T

57499954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71579572-G-A

57500034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71579504-G-A

57500632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71578750-G-T

57500691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71578693-C-T

57501489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71578174-T-C

57501507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71578157-T-C

57501628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71578075-G-C

http://identifiers.org/hco/15/GRCh38#57501795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71577928-A-C

http://identifiers.org/hco/15/GRCh38#57501911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71577829-C-A

57501977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71577768-C-T

57502417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71577424-G-A

57504936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71575404-A-G

57504936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71575404-A-T

57505119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71575221-G-A

57505248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71575098-G-A

57505319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71575033-A-G

57505470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574885-C-T

57505499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574858-C-G

57505546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574811-C-G

57505557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574799-C-T

57505586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574769-G-A

57505646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574706-A-G

57505678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574674-A-G

57505813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574558-G-A

57505931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574222-G-A

57505990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71574161-A-G

57506336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71573806-G-A

57506403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71573733-G-A

57507162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71573612-A-G

57507233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71573557-G-A

57507281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71573509-T-G

57507411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71573194-T-G

57507490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572698-T-C

57507490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572698-T-G

57507618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572543-A-G

57507657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572507-G-A

57507658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572506-G-A

57507854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572298-T-C

57507866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572286-A-G

57507916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572234-G-A

57507992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71572173-C-T

57509089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71571575-C-T

57509112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71571550-A-G

57509469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71571195-C-G

57509479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71571185-C-T

57509574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71571101-C-T

57509802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71570860-T-C

57509916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71570766-A-G

57510256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71568934-A-G

57510358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71568851-A-G

http://identifiers.org/hco/15/GRCh38#57510409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71568817-C-A

57510443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71568783-A-G

57510884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71568012-A-G

57511009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71567876-G-A

57511175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71567704-C-T

57511234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71567647-A-T

57511301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71567598-A-G

57511530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71567260-T-C

57511579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71567212-C-T

57511907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566934-A-G

57511991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566853-G-A

57512003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566843-T-A

57512155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566720-G-A

57512178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566705-G-A

57512178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566705-G-C

57512206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566677-T-C

57512227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566662-T-A

57512277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566612-T-A

57512338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566555-G-C

57512393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566505-G-A

57512393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566505-G-C

57512478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566397-A-T

57512494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566381-T-C

57512526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566349-G-T

57512537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566338-C-T

http://identifiers.org/hco/15/GRCh38#57512661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71566252-C-A

57512734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566179-T-C

57512771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566142-G-C

57512776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566137-C-G

57512871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71566051-C-T

57513223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71565571-A-G

57513316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71565532-G-C

57513350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71565505-G-A

57513350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71565505-G-T

57513521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71565341-T-C

57516715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71563589-C-T

http://identifiers.org/hco/15/GRCh38#57516735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71563568-C-A

57516739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71563564-G-A

57516739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71563564-G-C

57516739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71563564-G-T

57516855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: synonymous variant
orthologous variants: 71563457-C-T

57516886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71563426-G-A

57516891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71563421-G-A

57516936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71563376-G-A

57517027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71563291-G-T

57517047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71563274-G-A

http://identifiers.org/hco/15/GRCh38#57518280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71562728-C-A

57518280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562728-C-T

57518294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562714-A-G

57518576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562530-T-A

57518576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562530-T-C

http://identifiers.org/hco/15/GRCh38#57518579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71562527-C-A

57518579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562527-C-T

57518708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562401-C-G

57518873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562271-T-A

57519018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71562122-A-G

http://identifiers.org/hco/15/GRCh38#57519085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71562055-A-C

57519141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71561980-T-C

57519178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71561941-C-T

57519289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71561838-A-G

57519386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71561737-G-A

http://identifiers.org/hco/15/GRCh38#57521986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71560039-A-C

57522059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559962-G-A

http://identifiers.org/hco/15/GRCh38#57522123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71559580-C-A

57522123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559580-C-G

57522123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559580-C-T

57522227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559488-T-C

57522241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559478-A-T

57522321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559396-G-A

57522379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559337-T-G

http://identifiers.org/hco/15/GRCh38#57522420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71559295-C-A

57522445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559268-C-T

57522459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71559255-C-T

57523169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558930-C-T

57523382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558765-A-G

57523393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558754-T-C

57523448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558703-G-A

57523482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71558673-T-C

57523522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: stop gained
orthologous variants: 71558633-C-T

57523549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71558606-A-G

57523549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71558606-A-T

57523594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71558561-A-G

57523622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71558533-T-C

57523656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558498-G-A

http://identifiers.org/hco/15/GRCh38#57523675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71558478-C-A

57523676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558477-C-G

57523676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558477-C-T

http://identifiers.org/hco/15/GRCh38#57523712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71558455-C-A

57523712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558455-C-G

57523747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558421-G-T

http://identifiers.org/hco/15/GRCh38#57523749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71558419-A-C

57523757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558411-G-A

57523757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558411-G-T

http://identifiers.org/hco/15/GRCh38#57523759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71558409-C-A

57523762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558406-G-A

57523762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558406-G-C

57523762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558406-G-T

http://identifiers.org/hco/15/GRCh38#57523774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71558394-C-A

57523774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558394-C-G

57523907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558256-A-G

57524108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71558070-A-T

57524263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557940-C-T

http://identifiers.org/hco/15/GRCh38#57524431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71557785-C-A

57524431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557785-C-T

57524491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557752-A-G

57524564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557689-C-T

57524567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557686-G-A

57524568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557685-T-G

57524584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71557669-G-A

57524755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557498-A-G

http://identifiers.org/hco/15/GRCh38#57524800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71557449-C-A

57524874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557366-T-A

57524888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557360-A-T

57524934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557314-G-A

57525120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557138-G-C

57525123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71557133-T-G

57525634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71556074-G-A

57525783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71555917-T-A

57526139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71555581-T-G

http://identifiers.org/hco/15/GRCh38#57527037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71554074-C-A

57527110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71554016-A-G

57527274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553861-G-T

57527325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553824-A-G

57527331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553821-G-C

57527359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553797-A-G

http://identifiers.org/hco/15/GRCh38#57527412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71553765-C-A

57527412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553765-C-G

57527588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71553635-T-A

57527621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553618-T-C

57527623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553616-A-G

57527657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553588-G-A

57527657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71553588-G-T

57527697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 71553548-A-T

57527699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71553546-G-A

57527815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71553440-G-A

57527815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71553440-G-C

57527815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71553440-G-T

57528447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71553186-C-G

57528677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71552910-A-G

57528702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 71552885-G-A

57528831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552727-A-G

57528832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552726-G-A

57528832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552726-G-T

57528850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552698-G-A

http://identifiers.org/hco/15/GRCh38#57528863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71552685-C-A

57528863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552685-C-T

57528864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552684-T-A

57528864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552684-T-C

57528871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552643-C-T

57528936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71552544-A-G

57529010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552480-T-G

http://identifiers.org/hco/15/GRCh38#57529053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71552433-C-A

57529139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552374-G-A

57529139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552374-G-C

57529190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552327-G-A

57529239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552256-T-G

57529348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552166-T-A

57529426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552089-A-G

57529448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71552064-A-G

57529725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71551919-G-C

57529782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71551857-T-C

57529830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71551809-T-G

57529946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71551698-G-C

57530045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71551603-G-C

57530067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71551582-A-G

57530853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71549705-C-T

57531001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71549573-C-G

57531292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71549288-C-T

57531347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71549249-A-G

57531553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548846-T-C

http://identifiers.org/hco/15/GRCh38#57531578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71548821-A-C

57531578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548821-A-G

http://identifiers.org/hco/15/GRCh38#57531639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71548777-A-C

57531639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548777-A-T

57531661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548755-G-A

57531672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548747-T-A

57531794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548624-G-A

57531802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548612-T-A

57531803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548611-G-A

57531807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548607-G-A

57531807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548607-G-T

57531828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548586-G-T

57531908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548518-G-T

57531934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548492-T-C

57533027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548348-C-G

57533097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548281-C-T

57533444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71548004-G-T

57533697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71547757-C-G

57533934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71547576-G-T

57534287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71547158-T-G

57534361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71547082-G-A

57534619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71546659-C-T

57534830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71546467-C-T

57534907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71546384-T-A

http://identifiers.org/hco/15/GRCh38#57534997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71546293-A-C

57535241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71546057-T-G

57535396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545924-G-A

57535726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545659-C-T

57535739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545646-T-G

57535741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545644-G-A

57535806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545588-G-A

57535815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545579-A-G

57535824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545570-C-G

http://identifiers.org/hco/15/GRCh38#57535964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71545474-C-A

57535964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545474-C-G

57536502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545335-A-G

57536614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71545243-G-A

57536723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71544992-A-G

http://identifiers.org/hco/15/GRCh38#57537016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71544590-A-C

57537285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71544302-C-T

57537406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71544152-G-T

57537466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71544104-C-T

57537468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71544102-T-C

http://identifiers.org/hco/15/GRCh38#57537590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71544005-C-A

57537590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71544005-C-T

57538061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71543620-G-T

57538186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71543545-C-T

57538325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71543429-A-G

57538330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71543424-C-T

57538823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71542994-C-T

57538861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71542979-C-T

57538953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71542899-C-G

57539039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71542810-G-A

57539039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71542810-G-T

57539154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71542715-A-G

http://identifiers.org/hco/15/GRCh38#57539199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71542689-C-A

57539202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71542686-C-T

http://identifiers.org/hco/15/GRCh38#57541692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71542156-C-A

57543699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71539958-G-A

57543699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71539958-G-C

57544122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71539404-T-C

57544122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71539404-T-G

57544163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71539365-G-A

57544255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71539307-G-C

57544425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71539189-G-A

57544425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71539189-G-C

57544682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538953-G-A

57544683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538952-T-A

57544683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538952-T-C

57544962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538820-T-C

57544970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538807-C-T

57544972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538805-G-T

57545275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538563-T-G

57545385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538461-T-C

57545448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538399-T-A

57545448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538399-T-C

57545448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538399-T-G

http://identifiers.org/hco/15/GRCh38#57545455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71538391-A-C

57545455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538391-A-G

57545455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538391-A-T

http://identifiers.org/hco/15/GRCh38#57545495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71538358-C-A

57545495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538358-C-G

57545495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538358-C-T

57545507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538346-G-A

57545507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538346-G-T

57545534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538320-T-A

57545534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538320-T-G

57545729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538116-T-C

57545735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538110-A-G

57545750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538095-G-T

57545757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538088-G-T

57545798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538078-T-C

57545799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538077-G-T

http://identifiers.org/hco/15/GRCh38#57545812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71538064-C-A

57545812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538064-C-T

57545820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538057-T-C

57545954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538020-G-A

57545954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538020-G-T

57545955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538019-A-G

57545955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71538019-A-T

57545997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537999-G-A

57545997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537999-G-T

http://identifiers.org/hco/15/GRCh38#57546067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71537926-C-A

57546067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537926-C-G

http://identifiers.org/hco/15/GRCh38#57546068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71537925-C-A

57546068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71537925-C-T

57546069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71537924-G-A

57546112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense_variant, undefined
orthologous variants: 71537883-G-A

57546118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71537877-G-A

57546118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71537877-G-T

57546184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71537811-A-G

http://identifiers.org/hco/15/GRCh38#57546216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71537779-C-A

57546216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: synonymous variant
orthologous variants: 71537779-C-T

http://identifiers.org/hco/15/GRCh38#57546281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71537726-C-A

57546281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537726-C-T

57546359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537713-G-A

57546359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537713-G-C

57546359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537713-G-T

57546364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537708-C-T

57546366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537706-T-A

57546366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537706-T-C

57546367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537705-A-G

57546385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537687-G-A

57546506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537609-A-G

57546892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537310-T-G

57546920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71537282-G-C

57547265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71536761-G-A

57547265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: intron variant
orthologous variants: 71536761-G-T

57547383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71536644-G-T

57547384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71536643-A-T

57547398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71536632-G-A

57547398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71536632-G-C

57547398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: missense variant
orthologous variants: 71536632-G-T

57547530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536510-G-C

http://identifiers.org/hco/15/GRCh38#57547548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71536487-A-C

57547565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536470-G-A

57547565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536470-G-C

57547565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536470-G-T

57547799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536307-G-A

57547799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536307-G-T

57547924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536195-G-A

57547924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536195-G-T

57547935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536186-G-A

57547935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536186-G-C

57547935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536186-G-T

http://identifiers.org/hco/15/GRCh38#57548354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71536078-C-A

57548354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71536078-C-T

57548536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535959-G-T

57548613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535902-C-T

57548641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535881-A-G

http://identifiers.org/hco/15/GRCh38#57548692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71535835-C-A

57548747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535742-A-G

57548764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535724-G-A

57548764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535724-G-T

57548789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535699-G-T

57548923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535577-A-G

57548961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535547-G-A

57548961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535547-G-T

57549010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535513-G-T

57549025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535505-T-C

http://identifiers.org/hco/15/GRCh38#57549057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71535494-C-A

57549057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535494-C-T

57549069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535483-G-A

57549131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535438-A-G

57549187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535382-G-T

57549287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535353-T-C

57549331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535317-A-G

57549367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535282-T-C

57549431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535232-C-T

57549510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535157-G-T

57549518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535149-T-A

57549518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535149-T-C

57549609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535083-A-G

57549679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71535000-C-T

57549684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71534958-A-G

57549753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71534742-A-G

57549753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71534742-A-T

http://identifiers.org/hco/15/GRCh38#57550115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#71534379-C-A

57550115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71534379-C-T

57550494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25931
most severe consequence: 3 prime UTR variant
orthologous variants: 71534009-A-G