96518196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199381-T-C

96518314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199492-G-A

96518314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199492-G-T

96518378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199552-G-A

96518406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199580-C-T

http://identifiers.org/hco/10/GRCh38#96518452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41199617-C-A

96518623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199755-G-A

96518759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199862-C-T

96518803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199906-T-G

96518805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199908-T-C

96518913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41199997-C-T

96519295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200377-C-T

96519329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200410-A-G

96519360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200439-A-G

96519378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200457-T-G

96519394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200465-C-G

96519394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200465-C-T

96519871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200877-G-A

http://identifiers.org/hco/10/GRCh38#96519991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41200992-C-A

96519991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41200992-C-T

96520048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201035-G-T

96520253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201381-A-T

http://identifiers.org/hco/10/GRCh38#96520287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41201406-A-C

96520394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201497-T-C

http://identifiers.org/hco/10/GRCh38#96520439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41201541-A-C

96520439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201541-A-G

96520439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201541-A-T

96520508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201605-T-C

96520512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201609-T-C

96520571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201670-T-A

96520571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201670-T-C

http://identifiers.org/hco/10/GRCh38#96520582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41201677-C-A

96520582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201677-C-T

96520619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201714-G-A

96520619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201714-G-T

http://identifiers.org/hco/10/GRCh38#96520739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41201835-C-A

96520754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201850-C-T

96520788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41201891-T-C

96520820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202056-G-T

96521092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202338-T-C

http://identifiers.org/hco/10/GRCh38#96521222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41202461-A-C

96521222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202461-A-G

96521222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202461-A-T

http://identifiers.org/hco/10/GRCh38#96521251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41202491-A-C

96521517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202762-G-A

96521517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202762-G-T

96521555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202800-C-T

96521592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202837-T-A

96521592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202837-T-C

96521698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41202946-T-G

http://identifiers.org/hco/10/GRCh38#96521774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41203028-C-A

96521774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41203028-C-T

96521850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41203102-T-C

96522380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203635-T-A

96522380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203635-T-C

96522380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203635-T-G

http://identifiers.org/hco/10/GRCh38#96522406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41203660-C-A

96522406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203660-C-T

96522420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203674-G-A

96522420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203674-G-T

96522424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203680-T-C

http://identifiers.org/hco/10/GRCh38#96522426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41203682-C-A

96522426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203682-C-G

96522426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203682-C-T

96522452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203709-T-A

96522600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41203848-T-C

96522883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41204194-C-T

96522921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41204233-G-A

96523012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41204310-A-T

96523215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41204489-A-G

96523473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41204728-T-C

http://identifiers.org/hco/10/GRCh38#96526888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41205154-A-C

96527017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205286-T-A

http://identifiers.org/hco/10/GRCh38#96527082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41205327-A-C

http://identifiers.org/hco/10/GRCh38#96527118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41205365-C-A

96527118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205365-C-T

96527136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205384-A-G

96527337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205664-T-A

96527337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205664-T-G

http://identifiers.org/hco/10/GRCh38#96527370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41205693-A-C

96527567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205937-A-G

http://identifiers.org/hco/10/GRCh38#96527586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41205957-C-A

96527586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205957-C-G

96527586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41205957-C-T

96527674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41206036-A-G

96527799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41206161-T-C

96527811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41206175-T-C

96527868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41206218-T-C

96528308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41206865-G-A

96528308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41206865-G-C

96528308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41206865-G-T

96528622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41207206-C-T

http://identifiers.org/hco/10/GRCh38#96530448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41209576-C-A

http://identifiers.org/hco/10/GRCh38#96530479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41209616-C-A

http://identifiers.org/hco/10/GRCh38#96530713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41209847-A-C

96530714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41209848-G-A

96530714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41209848-G-T

96531014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41210144-G-C

96531167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41210288-T-C

96531226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41210345-C-T

96531236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41210355-T-C

96531312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41210416-T-C

96531506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41210586-G-A

http://identifiers.org/hco/10/GRCh38#96531721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41210831-C-A

96531737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41210859-T-C

96532868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211361-T-A

96532918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211410-G-T

96532921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211413-C-T

96533034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211507-T-C

96533326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211794-G-T

96533342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211810-A-G

96533371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211829-A-T

96533388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211846-T-C

96533499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41211953-T-C

96533662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41212096-G-A

96533775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41212230-T-C

96533955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41212403-T-C

96534089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41212595-G-C

96534089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41212595-G-T

96534178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41212681-C-G

96534259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41212775-T-C

96535048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41213774-T-C

96535143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41213863-T-A

96535471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41214758-T-A

96535471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41214758-T-C

96535614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41214891-A-G

96535635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41214908-A-G

96535673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41214927-G-A

96540332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41218122-C-T

96540351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41218140-T-C

96540369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41218157-G-A

96540495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41218234-T-G

96541202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41218968-C-T

96541206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41218972-C-T

96544000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41220707-T-C

96544020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41220727-T-C

96544020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41220727-T-G

96544048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41220754-G-C

96544060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41220766-G-A

96544295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221032-T-A

96544295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221032-T-C

96545381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221293-C-T

http://identifiers.org/hco/10/GRCh38#96545386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41221298-A-C

96545386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221298-A-T

96545540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221451-T-G

96545591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221492-T-C

96545596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221497-C-G

96545979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221535-T-C

96546101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221640-A-G

96546401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41221915-C-T

96546602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222108-C-T

96546748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222247-G-A

96546771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222286-G-A

96546771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222286-G-T

96547261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222734-T-C

96547353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222838-A-G

96547375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222860-C-T

96547452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222936-C-G

96547452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41222936-C-T

96547983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41223208-T-A

96547983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41223208-T-C

96548007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41223232-A-G

96548046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41223265-T-C

96548056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41223275-T-C

96548173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41223355-G-A

96548324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41223505-A-G

96548877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41224184-C-T

96549345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41224805-T-C

96549486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41224932-C-G

96549487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41224933-T-A

96549845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41225451-G-A

96550134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41225750-A-G

96550825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41226748-T-C

96550878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41226805-T-C

96551000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41226900-A-G

96551019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41226915-T-A

96551424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227308-A-G

96551441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227319-A-G

http://identifiers.org/hco/10/GRCh38#96551454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41227332-C-A

96551454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227332-C-T

96551490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227372-G-T

96551491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227373-T-A

96551491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227373-T-C

96551647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227496-G-A

96551734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227597-T-C

96552025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41227827-G-T

96552628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41228066-G-C

http://identifiers.org/hco/10/GRCh38#96552773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41228285-C-A

96552773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41228285-C-T

96552795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41228308-T-C

http://identifiers.org/hco/10/GRCh38#96552804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41228496-C-A

http://identifiers.org/hco/10/GRCh38#96553089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41229179-A-C

http://identifiers.org/hco/10/GRCh38#96553113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41229203-C-A

96553113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229203-C-T

96553162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229246-T-A

96553162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229246-T-G

96553164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229248-T-C

http://identifiers.org/hco/10/GRCh38#96553176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41229258-C-A

96553385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229448-C-T

96553586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229620-A-G

96553719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229751-T-C

96553826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41229828-C-G

http://identifiers.org/hco/10/GRCh38#96553829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41229849-C-A

96554143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41230159-T-C

http://identifiers.org/hco/10/GRCh38#96554636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41230634-C-A

96554652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41230650-A-G

96554813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41230797-A-G

96554976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41231161-C-T

96555298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41231470-T-C

96555667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41231848-A-T

96559046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233323-C-T

96559157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233415-C-T

96559540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233754-T-A

96559543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233757-G-T

http://identifiers.org/hco/10/GRCh38#96559578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41233792-C-A

96559578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233792-C-T

http://identifiers.org/hco/10/GRCh38#96559590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41233810-C-A

96559590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233810-C-G

96559590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233810-C-T

96559617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233842-T-C

96559680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41233904-A-T

96559719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41233943-T-A

96559719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41233943-T-C

96559758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233976-G-A

96559758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233976-G-C

96559758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233976-G-T

96559763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41233981-T-A

96559790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234007-T-G

http://identifiers.org/hco/10/GRCh38#96559812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41234029-A-C

96559833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234045-G-A

96559833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234045-G-T

96559877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234081-T-C

96559877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234081-T-G

96561237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234439-A-G

http://identifiers.org/hco/10/GRCh38#96561264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41234465-C-A

96561264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234465-C-T

96561539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234728-G-A

96561558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234743-C-T

http://identifiers.org/hco/10/GRCh38#96561565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41234750-C-A

96561577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234762-T-A

96561577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234762-T-G

96561652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41234827-A-T

96562086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41235190-A-G

96562190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41235294-T-A

96564668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41235736-T-G

96564854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41235902-A-G

96564970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236044-C-T

96564992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236066-A-G

http://identifiers.org/hco/10/GRCh38#96565145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41236210-C-A

http://identifiers.org/hco/10/GRCh38#96565190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41236256-C-A

96565190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236256-C-G

96565208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236274-A-T

96565215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236281-T-G

96565241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236305-T-A

96565275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236333-A-G

96565410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41236451-G-A

96565410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41236451-G-T

http://identifiers.org/hco/10/GRCh38#96565454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41236493-C-A

96565454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236493-C-T

96565473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236512-G-A

96565473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236512-G-C

96565473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236512-G-T

96565475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236514-T-A

96565475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236514-T-C

96565475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236514-T-G

96565481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236516-A-T

http://identifiers.org/hco/10/GRCh38#96565490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41236525-A-C

96565521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236557-G-A

96565521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236557-G-C

96565521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236557-G-T

96565522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236558-T-C

96565532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236565-T-C

96565576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236606-G-A

96565576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236606-G-C

96565576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236606-G-T

96565584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236614-T-C

96565584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236614-T-G

96565599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236632-G-T

96565678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236704-T-C

96565783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236786-T-C

96565890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236887-A-G

96566008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41236985-G-A

96568337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237143-A-G

96568345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237151-C-T

96568482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237283-T-C

96568612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237375-G-A

96568612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237375-G-C

96568745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237500-T-C

96568858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237615-C-G

96568858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237615-C-T

96568873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237633-C-G

96569368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41237860-C-T

96569673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41238118-T-C

http://identifiers.org/hco/10/GRCh38#96570052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41238474-C-A

96570130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41238571-T-C

96570222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41238653-T-C

96570423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41238926-G-C

96570492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41239043-G-A

96570526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41239094-T-C

96570621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41239189-T-C

96570958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41239512-C-G

96571220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41239902-A-T

96571319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41240050-C-T

96571504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41240226-C-G

96571576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41240296-G-A

96571576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41240296-G-C

96571576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41240296-G-T

96571896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41240590-T-A

96572038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41240892-G-A

96572366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41242170-C-G

http://identifiers.org/hco/10/GRCh38#96572461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41242259-C-A

96572461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41242259-C-G

http://identifiers.org/hco/10/GRCh38#96572468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41242266-C-A

96572965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41242485-T-C

96573000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41242520-C-T

http://identifiers.org/hco/10/GRCh38#96573099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41242645-A-C

96573233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41242939-C-T

http://identifiers.org/hco/10/GRCh38#96573338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41243023-C-A

96573404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243085-T-C

96573427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243106-C-T

96573565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243235-T-A

96573695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243354-T-C

96573696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243355-T-C

96575255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243580-G-A

http://identifiers.org/hco/10/GRCh38#96575444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41243767-C-A

96575468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243782-G-C

96575666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243942-T-C

96575683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41243962-G-A

96575782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244050-T-C

96575855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244125-T-C

96575946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244198-G-T

96576187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244410-G-A

96576203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244423-T-C

96576209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244429-T-C

96576862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244795-A-T

96576899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244822-T-C

96576969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244885-G-T

96576974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41244890-T-C

96577375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41245234-A-G

96577526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41245374-G-C

96577544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41245395-G-C

96580618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41245941-C-T

http://identifiers.org/hco/10/GRCh38#96580679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41246001-A-C

http://identifiers.org/hco/10/GRCh38#96580692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41246014-A-C

96580692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41246014-A-G

96580693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41246015-C-T

96581008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41246432-T-C

96581011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41246435-A-G

http://identifiers.org/hco/10/GRCh38#96581077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41246501-C-A

96581618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41247055-G-A

96581788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41247462-C-T

96581793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41247467-T-C

96582065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41247730-G-C

96582099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41247772-T-A

96582099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41247772-T-C

96584165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41249806-G-C

http://identifiers.org/hco/10/GRCh38#96584184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41249829-A-C

96584184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41249829-A-G

96584352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41249984-G-A

96584582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41250219-C-T

96584594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41250226-G-A

http://identifiers.org/hco/10/GRCh38#96584689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41250305-C-A

96585392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41250959-A-T

96585579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41251158-G-C

96585783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41251337-T-C

96586150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41251723-C-G

96586226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41251795-G-A

http://identifiers.org/hco/10/GRCh38#96586672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41252130-C-A

96586672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41252130-C-T

96586691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41252149-G-A

96586691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41252149-G-T

96586707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41252165-G-A

96586707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41252165-G-T

96586722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41252186-G-A

96586722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41252186-G-C

96586722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41252186-G-T

96586778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41252242-G-A

96586778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, missense_variant
orthologous variants: 41252242-G-C

96586778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, missense_variant
orthologous variants: 41252242-G-T

96586814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, missense_variant
orthologous variants: 41252272-G-A

96586814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, missense_variant
orthologous variants: 41252272-G-C

96586814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, missense_variant
orthologous variants: 41252272-G-T

http://identifiers.org/hco/10/GRCh38#96586880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41252338-C-A

96586880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41252338-C-G

96586880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41252338-C-T

96587181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252588-C-G

96587181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252588-C-T

96587209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252615-G-A

96587244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252646-G-A

96587244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252646-G-C

96587262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252655-G-A

96587287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252661-G-A

96587287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252661-G-C

96587287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252661-G-T

96587288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41252662-G-T

http://identifiers.org/hco/10/GRCh38#96587324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41252683-C-A

96587324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41252683-C-T

96587410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41252716-T-A

http://identifiers.org/hco/10/GRCh38#96587449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41252733-C-A

96587449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21529
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41252733-C-T