24804705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52530748-C-G

24804774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52530809-T-C

24804931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52530932-A-G

24805287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52531242-G-C

24805418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52531371-C-T

24805632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52531556-C-T

24806095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52531971-A-G

24806176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52532051-G-T

24806265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52532116-C-T

24806319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52532151-C-T

24806528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52532350-G-T

24806646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52532474-T-C

24806689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52532504-T-G

24807421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52532686-G-A

http://identifiers.org/hco/4/GRCh38#24807497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52532753-C-A

24807802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533004-G-T

http://identifiers.org/hco/4/GRCh38#24807874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52533058-C-A

24807874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533058-C-T

http://identifiers.org/hco/4/GRCh38#24807953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52533137-C-A

24807953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533137-C-T

24808098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533288-G-A

24808098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533288-G-T

24808125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533315-G-A

24808125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533315-G-T

24808172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533362-G-C

24808194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533384-G-A

24808194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533384-G-T

24808239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533427-T-A

24808239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533427-T-C

24808239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533427-T-G

http://identifiers.org/hco/4/GRCh38#24808264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52533452-C-A

24808264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533452-C-T

24808297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533489-G-A

24808297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533489-G-T

24808309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533501-G-A

24808309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533501-G-T

24808313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533505-G-A

24808339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3 prime UTR variant
orthologous variants: 52533541-G-T

24808404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 52533605-G-A

http://identifiers.org/hco/4/GRCh38#24808405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52533606-C-A

24808405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 52533606-C-T

24808440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 52533641-G-A

24808440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 52533641-G-T

24808546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 52533747-G-A

24808546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 52533747-G-T

24808593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 52533794-C-T

24808628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 52533829-T-C

24808712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52533916-G-A

24808712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52533916-G-C

24808712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52533916-G-T

24808765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52533969-G-A

24808784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52533988-C-T

24808862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534061-T-C

http://identifiers.org/hco/4/GRCh38#24808894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52534090-C-A

24808894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534090-C-T

24809158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534182-G-T

24809330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534334-T-G

24809387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534395-T-A

24809464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534468-A-G

24809611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534640-C-G

24809732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534754-T-C

24809849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534871-G-A

24809905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534921-G-A

24810019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535033-T-A

24810057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535094-C-G

24813954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537433-T-C

24814101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537582-G-A

24814304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537759-G-T

24814343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537792-G-C

24814369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537815-T-C

24814434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537880-C-T

24814459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537886-T-C

24814503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537919-T-C

24814630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538020-T-C

24814687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538077-T-C

24814740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538128-G-A

24814801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538169-C-T

http://identifiers.org/hco/4/GRCh38#24814846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52538214-C-A

http://identifiers.org/hco/4/GRCh38#24814937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52538301-A-C

24815208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538662-T-C

24815231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538685-G-A

http://identifiers.org/hco/4/GRCh38#24815238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52538692-C-A

24815402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538850-C-T

24815433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538881-G-A

http://identifiers.org/hco/4/GRCh38#24815603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52539050-A-C

24815851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52539342-G-C

24815851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52539342-G-T

24815858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52539349-C-T

24816831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540047-T-C

24816908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540118-T-A

24816942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540154-C-T

24817053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540262-G-A

24817164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540362-G-A

24817593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540666-T-C

http://identifiers.org/hco/4/GRCh38#24817757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52540746-A-C

24818164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52541124-G-A

24819990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52542577-A-G

24820000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52542587-A-G

24820008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52542595-T-C

24820028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52542615-T-C

24820263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52547652-C-T

24820366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52547764-G-A

24820372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52547770-C-G

24820372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52547770-C-T

24820509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52547890-A-G

24820557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52547935-A-G

24820658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52548027-C-T

24820915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52548283-A-T

http://identifiers.org/hco/4/GRCh38#24820918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52548286-C-A

24820918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52548286-C-T

24821003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52548376-T-A

24821017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52548389-T-A

24821017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52548389-T-C

24821065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52548441-T-A

24821065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52548441-T-C

24821104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548479-G-A

24821104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548479-G-C

http://identifiers.org/hco/4/GRCh38#24821208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52548584-C-A

24821208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548584-C-T

http://identifiers.org/hco/4/GRCh38#24821224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52548600-C-A

24821253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548629-C-T

24821380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548762-C-T

24821659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549043-A-G

24821822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549216-T-C

24821823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549217-G-C

24821874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549267-T-C

24821880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549273-T-A

24821953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549354-G-A

24821954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549355-T-C

24822213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549727-A-T

24822292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549806-C-T

24822347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549871-G-T

24822469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549984-A-G

24822469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549984-A-T

24822475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549990-G-A

24822475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549990-G-C

24822475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549990-G-T

24822498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 52550014-T-C

24822498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 52550014-T-G

24822588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550103-G-A

24822588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550103-G-C

24822647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550154-T-C

http://identifiers.org/hco/4/GRCh38#24822651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52550157-C-A

24822651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550157-C-T

24822700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550197-T-C

24822701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550198-G-T

24822785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550274-T-A

24822822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550311-G-T

http://identifiers.org/hco/4/GRCh38#24822836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52550323-C-A

24822836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550323-C-G

24822836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550323-C-T

24822886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550373-G-A

24822886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550373-G-C

24822888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550375-G-T

24822963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52550447-A-G

24823264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52550901-G-A

24823264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52550901-G-T

24823279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52550926-C-T

24823334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52550979-T-C

24823645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52551273-T-C

24823831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52551454-C-G

24823911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52551534-C-T

24823912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52551535-C-T

24825219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52552587-G-A

24825365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52552721-G-A

http://identifiers.org/hco/4/GRCh38#24825415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52552794-A-C

24825917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron variant
orthologous variants: 52552985-T-C

24827564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554530-A-G

24827620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554579-A-G

24827644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554600-G-A

24827644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554600-G-T

24827695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554646-T-C

24827713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554663-G-A

http://identifiers.org/hco/4/GRCh38#24827743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52554690-C-A

24827743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554690-C-G

24827743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554690-C-T

24827777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554729-T-C

http://identifiers.org/hco/4/GRCh38#24827830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52554783-C-A

24827852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554809-G-A

24827904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554835-T-C

24827959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554869-T-C

24828089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554936-C-T

24828133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52554965-C-G

24828232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52555047-G-A

http://identifiers.org/hco/4/GRCh38#24828262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52555087-C-A

24828265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52555096-G-A

24828265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52555096-G-T

http://identifiers.org/hco/4/GRCh38#24828361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52555174-C-A

24831004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52556959-C-T

http://identifiers.org/hco/4/GRCh38#24831020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52556969-C-A

http://identifiers.org/hco/4/GRCh38#24831022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52556971-C-A

24831022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52556971-C-G

24831079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557018-G-A

24831079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557018-G-T

http://identifiers.org/hco/4/GRCh38#24831081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52557020-C-A

24831081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557020-C-T

24831118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557055-T-C

24831213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557128-G-A

24831213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557128-G-T

24831215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557130-C-T

http://identifiers.org/hco/4/GRCh38#24831261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52557168-C-A

24831261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557168-C-T

24831283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557201-G-T

24831287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557205-T-C

24831352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557260-G-A

24831364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557272-T-C

24831459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52557399-C-T

24831498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 52557419-C-T

24831561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52557482-A-G

24831665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557584-A-G

24831765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557682-T-C

http://identifiers.org/hco/4/GRCh38#24831860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52557883-A-C

24831860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557883-A-G

24831876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557907-A-G

24834225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559391-A-G

http://identifiers.org/hco/4/GRCh38#24834444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52559602-C-A

24834444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559602-C-T

24834501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559684-G-A

24834714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559858-A-G

24834796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559935-G-A

24834796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559935-G-C

24834796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559935-G-T

http://identifiers.org/hco/4/GRCh38#24834802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52559941-C-A

http://identifiers.org/hco/4/GRCh38#24834873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52559982-C-A

24834873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559982-C-T

24834879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559988-T-C

24834879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559988-T-G

24834923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560025-T-A

24834923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560025-T-C

24834927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560029-T-C

24834996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52560097-C-T

24835048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560149-G-A

24835048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560149-G-T

http://identifiers.org/hco/4/GRCh38#24835091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52560193-C-A

24835091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560193-C-T

24835124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560226-A-G

http://identifiers.org/hco/4/GRCh38#24835127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52560229-C-A

24835127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560229-C-G

24835127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560229-C-T

24835567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52560653-G-A

24836246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561281-C-G

24836253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561289-G-A

24836310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561342-A-G

24836319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561351-T-A

24836319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561351-T-C

24836320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561352-A-G

http://identifiers.org/hco/4/GRCh38#24836379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52561411-A-C

24836379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561411-A-G

24836430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561453-T-A

24836430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561453-T-C

24836431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561454-G-T

24836571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561604-T-A

http://identifiers.org/hco/4/GRCh38#24836641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52561663-C-A

24836772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561791-G-C

24837084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562095-T-C

24837118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562129-T-C

24837166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562177-G-A

24837166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562177-G-T

http://identifiers.org/hco/4/GRCh38#24837167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52562178-C-A

24837178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562189-G-A

24837186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562275-C-G

24837186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562275-C-T

24837189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562278-G-A

24837189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562278-G-T

http://identifiers.org/hco/4/GRCh38#24837198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52562287-C-A

24837198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562287-C-T

24837207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562296-G-C

24837207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562296-G-T

http://identifiers.org/hco/4/GRCh38#24837242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52562392-C-A

24837278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52562428-A-G

24837337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52562487-G-A

24837337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52562487-G-T

24837380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52562530-G-A

24837380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52562530-G-C

24837380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52562530-G-T

24837425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562567-C-T

24837487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562628-G-C

http://identifiers.org/hco/4/GRCh38#24837536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52562674-C-A

24837536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562674-C-T

24837667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562812-C-T

24837696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562841-T-C

24837755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562892-G-A

24837795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562945-T-C

24837805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562955-C-T

24837927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563078-T-C

24838005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563142-G-T

24838080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563243-G-A

24838080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563243-G-T

24838099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563265-G-T

24838142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563304-A-G

24838149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 52563311-T-G

24838174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52563336-T-C

24838335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563506-C-G

24838360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563538-A-G

24838373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563547-T-A

http://identifiers.org/hco/4/GRCh38#24838402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52563575-A-C

24838419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563592-T-C

http://identifiers.org/hco/4/GRCh38#24838648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52563814-A-C

http://identifiers.org/hco/4/GRCh38#24838759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52563916-C-A

24839678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52564066-A-G

24839699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52564087-C-T

24839725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52564113-A-G

24840015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52564337-A-G

24840025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52564347-G-A

24840407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52564615-C-T

24840509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52564677-G-A

24840743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52565996-A-G

http://identifiers.org/hco/4/GRCh38#24840885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52566141-C-A

http://identifiers.org/hco/4/GRCh38#24840960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52566211-A-C

24841008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566257-G-A

24841203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566445-G-A

24841203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566445-G-T

24841743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566916-C-T

24841954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567080-C-T

24842112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567255-T-G

http://identifiers.org/hco/4/GRCh38#24842141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52567269-C-A

24842141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567269-C-T

24842235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567366-G-A

24842325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567522-G-A

24842336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567529-C-T

24842368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567561-C-G

24842368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567561-C-T

24842405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567591-T-C

24842431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567616-A-G

http://identifiers.org/hco/4/GRCh38#24842493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52567671-C-A

24842546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567713-G-A

24842632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567799-T-C

24842701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567867-G-C

24842734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567907-C-T

http://identifiers.org/hco/4/GRCh38#24842869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52568039-C-A

24842869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568039-C-T

24842919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568091-C-T

24846516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52569998-A-T

24846565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570047-C-T

24846617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570095-C-T

24846946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570363-G-A

24847162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570561-A-T

24847466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570808-A-G

24847508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570848-T-C

24849822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52572672-C-G

24849822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52572672-C-T

24849921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52572755-G-A

24849983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52572817-C-T

http://identifiers.org/hco/4/GRCh38#24850010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52572850-C-A

24850224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52573126-C-G

24850227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52573129-T-C

24850334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52573222-C-T

24850379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52573263-A-G

24850611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52573461-G-A

24850717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52573566-C-T

http://identifiers.org/hco/4/GRCh38#24850899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#52573796-C-A

24850980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52573899-A-G

http://identifiers.org/hco/4/GRCh38#24851090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52573979-C-A

24851556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52574579-G-A

24851556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52574579-G-T

24851855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52574831-G-A

24851893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52574870-T-A

24851893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52574870-T-C

24851944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52574907-C-G

24852134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577148-T-C

24852330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577332-A-T

24852423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577427-G-C

http://identifiers.org/hco/4/GRCh38#24852992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52577992-C-A

24852992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577992-C-T

24853033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52578036-G-C

24853033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52578036-G-T

24853093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52578095-T-G

http://identifiers.org/hco/4/GRCh38#24853223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52578223-A-C

24853255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52578253-G-T

http://identifiers.org/hco/4/GRCh38#24853324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52578320-C-A

24853654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52579116-A-G

24853864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52579843-C-T

24853880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52579859-T-C

24854119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52580174-C-T

24854252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52580301-C-T

24854569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52580529-C-T

24854888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52580791-C-T

24855191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581095-C-T

24855703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581236-C-G

24855795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581328-G-A

24855913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581422-T-C

24855913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581422-T-G

24855974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581455-C-G

24856031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581520-G-C

24856034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581523-T-G

24856065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581554-G-T

24856197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581662-C-T

24856323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581772-T-C

24856362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581799-C-T

24856407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52581847-T-C

24856631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582006-G-A

24856660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582034-C-T

24856661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582035-A-G

24856665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582039-G-T

24856832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582144-T-C

24856914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582217-C-T

24856997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582329-A-G

24857431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582679-A-G

24857666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52582905-A-T

24857843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52583095-C-T

http://identifiers.org/hco/4/GRCh38#24857880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52583132-C-A

24857880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52583132-C-T

24857935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52583183-C-T

24858009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52583255-C-T

24858097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52583337-G-C

24858352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52583583-G-A

24865068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52585734-T-C

24865338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52586002-C-T

http://identifiers.org/hco/4/GRCh38#24865597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52586249-C-A

24865697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52586335-T-G

24865817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52586557-T-C

24865899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52586624-G-C

24866133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52586854-T-C

24866284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52587004-C-T

24866536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52587262-C-T

24866546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52587272-C-T

24867973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52588785-C-G

24867973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52588785-C-T

24868061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52588874-G-C

http://identifiers.org/hco/4/GRCh38#24868155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52588966-C-A

24868204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52589013-C-G

24868576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52589395-A-G

http://identifiers.org/hco/4/GRCh38#24868642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52589451-C-A

24869062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52589838-C-T

24869284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52590073-C-T

24869312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52590101-G-A

24869346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52590146-T-C

24869408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52590250-C-T

24869531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52590379-G-A

http://identifiers.org/hco/4/GRCh38#24869915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52590571-C-A

24870157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52590781-T-C

24870476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52591134-C-T

http://identifiers.org/hco/4/GRCh38#24871598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52592160-A-C

http://identifiers.org/hco/4/GRCh38#24871812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52591264-C-A

24871814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52591266-G-T

http://identifiers.org/hco/4/GRCh38#24872140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52592533-C-A

24872311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52592677-G-T

24872332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52592698-G-T

24873738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593097-T-A

24873738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593097-T-C

24873765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593123-T-C

http://identifiers.org/hco/4/GRCh38#24873789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52593152-C-A

http://identifiers.org/hco/4/GRCh38#24873860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52593218-C-A

24873860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593218-C-T

24873881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593240-T-A

24873914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593255-A-G

24873932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593271-T-C

24873951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593288-A-G

24873975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52593315-C-T

24874821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52594576-A-G

24876723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52596581-T-C

http://identifiers.org/hco/4/GRCh38#24876757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52596615-C-A

24876763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52596625-G-A

24876763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52596625-G-T

24877071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597148-C-T

http://identifiers.org/hco/4/GRCh38#24877076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52597153-A-C

24877374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597250-T-C

24877543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597314-T-C

24877638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597421-T-G

24877729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597520-G-A

24877779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597563-A-G

24877843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597624-T-A

24877858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597639-C-T

24877859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597640-G-A

24877949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52597727-G-T

24878286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52598053-C-G

24878793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52598509-T-A

24878921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52598616-C-T

24878960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52598652-T-G

24879023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52598714-G-A

24879131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52599466-G-A

24884778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601374-A-G

24884825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601403-T-C

24884914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601492-C-T

24884936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601514-G-A

24884950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601531-T-C

24884967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601548-G-C

24885213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601747-C-T

24885428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601942-A-T

24885466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52601980-G-A

24885952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52602499-C-T

24886069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52602620-A-G

24886252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52602795-G-A

24886254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52602797-G-A

24886683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603146-T-C

24886684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603147-G-C

24886760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603228-G-T

24886849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603303-A-G

24886851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603305-C-T

24887083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603517-T-C

24887292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603741-G-C

24887362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603801-T-G

24887381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603819-C-T

24887466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603902-T-G

24887480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52603916-C-G

24887616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52604421-T-C

24887761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52604566-T-C

24887799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52604622-C-T

24887837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52604698-G-C

24887912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52604771-G-A

24888649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52605916-T-A

24888733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52605998-A-T

24888734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52605999-C-T

24888803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606064-G-A

24888875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606135-A-G

24888949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606204-C-T

24889226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606475-C-T

24889233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606482-T-C

24889374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606628-G-A

24889486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606738-A-G

24889531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52606787-C-T

24890112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52607604-T-G

24890572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52608175-A-G

24891200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52608782-C-G

24891200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52608782-C-T

24891318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52608885-G-A

24891344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52608905-G-C

24891352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52608913-C-T

24891403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52608964-A-T

24891500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52609055-A-G

24891609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52609140-C-T

24894658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52611477-G-A

24894658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52611477-G-T

24895402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52611859-T-G

24895410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52611866-G-A

http://identifiers.org/hco/4/GRCh38#24895631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52612098-A-C

http://identifiers.org/hco/4/GRCh38#24895939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52612372-C-A

24896293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52612811-C-T

24896305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52612823-C-T

24896332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52612850-C-T

24896424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52612944-T-C

24896478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613228-A-G

24896487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613235-G-C

24896518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613272-G-A

24896520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613274-G-A

24896565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613309-A-G

24896653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613393-T-C

24896918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613653-T-G

24896974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613709-T-C

24897172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613920-T-G

24897311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52613988-G-A

http://identifiers.org/hco/4/GRCh38#24897363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52614041-A-C

24897370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614048-G-A

24897503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614180-G-T

24897818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614458-G-A

24897827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614466-G-A

24897842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614480-G-T

24897866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614502-C-T

24897949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614578-G-C

24897949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52614578-G-T

24898419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52615034-T-C

24900767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52615709-G-A

24901338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52617100-G-A

24901358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52617119-G-A

24901394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52617155-A-G

24902282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52618757-G-C

24902446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52618907-C-T

http://identifiers.org/hco/4/GRCh38#24902586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52619045-A-C

24903043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619368-A-G

24903069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619395-G-A

24903069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619395-G-T

24903080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619406-T-G

24903086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619412-C-T

24903097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619423-T-C

24903243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619560-C-G

24903243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619560-C-T

24903434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52619730-G-A

24903762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52620020-G-T

24907340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622961-C-G

24907618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623434-C-T

24907679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623516-T-A

24908280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623994-C-T

http://identifiers.org/hco/4/GRCh38#24909009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52625106-C-A

24909069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52625156-G-A

24909568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52625611-G-C

24910191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626137-A-G

24910244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626190-T-C

http://identifiers.org/hco/4/GRCh38#24910273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52626218-A-C

http://identifiers.org/hco/4/GRCh38#24910360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52626310-A-C

24910410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626360-G-C

24910492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626431-T-G

24910644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626568-T-C

24910700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626611-A-G

24910722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626628-A-G

24910943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626860-T-G

24911019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626978-T-C

24911019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52626978-T-G

24911108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627114-G-A

24911432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627487-C-G

24911509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627698-C-T

24911511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627700-C-G

24911511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627700-C-T

24911603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627805-A-G

24912026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627981-G-A

24912034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627989-G-A

24912034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52627989-G-C

24912079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628033-A-G

24912239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52628167-T-G

http://identifiers.org/hco/4/GRCh38#24912692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628609-C-A

24912692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628609-C-T

24912750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52628640-G-A

24912750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52628640-G-T

http://identifiers.org/hco/4/GRCh38#24912760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628650-C-A

24912760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628650-C-G

24912760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628650-C-T

http://identifiers.org/hco/4/GRCh38#24912792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628668-C-A

24912792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628668-C-G

24912792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628668-C-T

24912798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628674-G-A

24912798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628674-G-C

24912798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628674-G-T

http://identifiers.org/hco/4/GRCh38#24912842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628718-C-A

24912842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 52628718-C-G

24912842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 52628718-C-T

http://identifiers.org/hco/4/GRCh38#24912888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628763-C-A

24912888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628763-C-G

24912888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628763-C-T

http://identifiers.org/hco/4/GRCh38#24912904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628782-C-A

24912904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628782-C-T

http://identifiers.org/hco/4/GRCh38#24912912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628790-C-A

24912912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628790-C-G

24912912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628790-C-T

http://identifiers.org/hco/4/GRCh38#24912915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628793-C-A

24912915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628793-C-G

24912915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628793-C-T

http://identifiers.org/hco/4/GRCh38#24912936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628815-C-A

24912936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52628815-C-T

24912976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628855-G-A

24912976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628855-G-C

24912976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628855-G-T

http://identifiers.org/hco/4/GRCh38#24912977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628856-C-A

24912977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628856-C-T

http://identifiers.org/hco/4/GRCh38#24912996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628875-C-A

24912996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628875-C-G

24912996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628875-C-T

http://identifiers.org/hco/4/GRCh38#24913012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52628891-C-A

24913012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52628891-C-T

24913148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52628999-C-T

http://identifiers.org/hco/4/GRCh38#24913276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#52629142-A-C

24913934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630045-C-G

24914022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630134-A-T

24914029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630141-G-T

24914199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630269-G-T

24914482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630492-C-T

24914723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630668-A-G

24914766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630713-G-C

24914788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630767-G-A

http://identifiers.org/hco/4/GRCh38#24914847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52630959-A-C

24914866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631092-A-G

http://identifiers.org/hco/4/GRCh38#24915427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52631631-A-C

24915846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632043-T-C

http://identifiers.org/hco/4/GRCh38#24915928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52632125-C-A

24916007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632212-C-T

24916047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632252-G-A

http://identifiers.org/hco/4/GRCh38#24916050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52632254-A-C

24916051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632255-G-C

24916259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632648-G-A

24916295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632684-C-T

24916310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632699-G-A

24916310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632699-G-C

24916310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632699-G-T

24916404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632795-A-T

24916497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632941-A-G

http://identifiers.org/hco/4/GRCh38#24916503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52632947-C-A

24916503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632947-C-T

24916785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633309-A-T

24916823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633341-T-C

24916830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633348-A-G

24917131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633629-G-C

24917156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633653-G-A

24917257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633750-G-A

24917257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633750-G-C

24917651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52634137-C-T

24917956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634427-G-C

24918053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634523-A-G

24918365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634823-G-A

24918451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634911-G-A

24918451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634911-G-T

24918461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634920-C-T

24918537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634995-T-A

24918566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635024-A-G

http://identifiers.org/hco/4/GRCh38#24921383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52640272-C-A

24921384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640273-C-G

24921384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640273-C-T

http://identifiers.org/hco/4/GRCh38#24921398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52640287-C-A

24921398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640287-C-G

24921853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640688-T-G

24921866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640701-T-A

24921942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640774-G-T

24922121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640926-T-C

24922134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640939-G-A

24922178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640985-G-A

24922178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52640985-G-T

24922237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52641087-A-G

24922333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52641135-C-T

http://identifiers.org/hco/4/GRCh38#24922551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52641324-C-A

24922551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52641324-C-T

24922637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52641408-G-A

24923353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642085-A-G

24923646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642373-T-A

24923674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642399-G-A

24923766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642488-C-T

24924097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643053-C-T

24924188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642986-G-A

24924499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642698-G-A

http://identifiers.org/hco/4/GRCh38#24926275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52644540-A-C

24926944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645144-C-T

24926954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645155-G-A

24927159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645357-G-A

24927742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645915-C-T

24928076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52646915-G-A

24929124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52648293-G-C

24929238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52648400-G-A

24929238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52648400-G-T

24929507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52648650-T-G

24929594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52648734-C-T

24929683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52648821-C-T

24929717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52648855-C-T

24930716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52650752-C-G

http://identifiers.org/hco/4/GRCh38#24930811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52650846-A-C

24930885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52650926-G-A

24930885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52650926-G-C

24931312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52651554-T-A

24931415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52651675-C-T

24931539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52651812-T-A

24931622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52651916-C-G

24931622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52651916-C-T

24931763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52652174-T-C

24932000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52652397-T-C

24932025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52652414-A-G

http://identifiers.org/hco/4/GRCh38#24932076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52652440-C-A

http://identifiers.org/hco/4/GRCh38#24932087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52652451-C-A

24932106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52652468-C-T

24932250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52652599-T-A

24932358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52652698-A-G

24932383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52652724-G-C

24932719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52653052-A-G

24937833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52654631-C-T

24937937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52654747-G-T

24938069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52655237-T-C

http://identifiers.org/hco/4/GRCh38#24938093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52655279-A-C

24938185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52655370-G-C

24938196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52655381-A-G

24944933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52655752-C-T

24945221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52656016-T-G

24945377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52656249-G-T

http://identifiers.org/hco/4/GRCh38#24945477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52656346-C-A

24946157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52656853-C-T

24946196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52656892-G-A

24946303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52657000-G-A

24946372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52657094-T-C

24946638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52657842-A-G

24946832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52658039-T-A

24946915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52658090-C-T

24947881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52658651-G-A

24948029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52658799-C-G

24948029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52658799-C-T

24948098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52658867-A-G

24951048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662029-G-T

24951099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662077-G-A

24951102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662080-G-A

24951165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662142-G-A

http://identifiers.org/hco/4/GRCh38#24951385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52662386-A-C

24951705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662709-G-A

24951705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662709-G-C

24951705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662709-G-T

24951711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52662715-A-G

http://identifiers.org/hco/4/GRCh38#24951867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52662851-A-C

24955375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52663365-G-T

24955398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52663387-T-C

24955460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52663446-C-G

http://identifiers.org/hco/4/GRCh38#24955512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52663487-C-A

24955668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52663764-G-A

24955687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52663783-G-C

http://identifiers.org/hco/4/GRCh38#24955736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52663832-A-C

24955895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52663928-A-G

24956073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664034-C-T

http://identifiers.org/hco/4/GRCh38#24956157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52664109-A-C

24956254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664205-A-T

24956260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664211-C-G

24956285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664234-T-C

24956392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664339-T-C

24956479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664423-T-G

24956581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664505-G-A

24956825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664746-G-C

24956999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52664893-C-T

24957185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665049-T-C

http://identifiers.org/hco/4/GRCh38#24957233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52665100-A-C

24957237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665105-A-G

24957354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665217-A-G

24957410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665274-T-G

24957637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665400-T-C

24957697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665457-G-A

24957740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665510-G-A

24958009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665761-G-T

24958182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665900-T-C

24958225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665939-C-G

24958225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52665939-C-T

24958294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52666007-C-T

24973987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52666941-C-G

24974088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52667028-A-G

24974174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52667114-G-A

24974207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52667139-A-G

24974293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52667235-C-T

24974313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52667255-C-T

24979006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52669899-G-A

24979014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52669915-G-A

24979426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52670287-G-C

24979632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52670500-C-G

24979675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52670568-G-A

24979700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52670592-A-G

24979730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52670622-T-C

24979752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52670644-T-C

24980060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52672579-G-T

http://identifiers.org/hco/4/GRCh38#24980073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#52672591-C-A

24980073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52672591-C-G

24980073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52672591-C-T

24980100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52672618-G-A

24980100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25405
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52672618-G-T