http://identifiers.org/hco/4/GRCh38#38867757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65127414-C-A

38867757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65127414-C-G

38867822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65127475-G-C

38867822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65127475-G-T

http://identifiers.org/hco/4/GRCh38#38867860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65127513-C-A

38867860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65127513-C-T

38867974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127589-G-A

38867974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127589-G-C

38867974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127589-G-T

38868005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127620-G-A

38868005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127620-G-T

38868162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127777-G-A

38868162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127777-G-T

http://identifiers.org/hco/4/GRCh38#38868174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65127782-C-A

38868174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127782-C-T

38868190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127791-T-C

38868280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127876-G-A

38868319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127917-T-C

38868333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127931-G-A

38868333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127931-G-T

38868339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127937-G-A

http://identifiers.org/hco/4/GRCh38#38868376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65127970-C-A

38868376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127970-C-T

http://identifiers.org/hco/4/GRCh38#38868386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65127980-C-A

38868386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65127980-C-T

http://identifiers.org/hco/4/GRCh38#38868414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65128010-C-A

38868414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65128010-C-T

http://identifiers.org/hco/4/GRCh38#38868439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65128036-C-A

38868552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128145-T-C

38868577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128171-G-A

38868577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128171-G-T

38868620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128212-T-C

38868777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128348-T-A

38869063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128653-A-G

38869082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128672-T-C

38869252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65128833-C-T

38869470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65129173-T-C

38869884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65129640-T-G

38870002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65129733-A-G

38870026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65129756-G-T

38870430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65130234-C-G

http://identifiers.org/hco/4/GRCh38#38870947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65130696-C-A

38871553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65131155-A-G

38871554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65131156-C-G

38872131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65131699-G-C

http://identifiers.org/hco/4/GRCh38#38872507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65132203-C-A

38872616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65132372-C-T

38872677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65132436-T-C

38872924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65132681-T-G

38872953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65132712-T-G

http://identifiers.org/hco/4/GRCh38#38873054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65132813-C-A

38873119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65132874-G-C

38873123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65132878-C-T

http://identifiers.org/hco/4/GRCh38#38873182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65132937-A-C

http://identifiers.org/hco/4/GRCh38#38873448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65133198-C-A

38873625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65133418-G-A

38873716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65133793-G-C

38873778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65133899-G-A

http://identifiers.org/hco/4/GRCh38#38873826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65133937-A-C

38874131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65134171-C-T

38874205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65134244-C-T

38874277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65134316-C-T

38878062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65137042-T-A

38878174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65137157-G-A

38878206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65137189-C-T

38878229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 65137212-G-T

38878250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65137233-G-C

38878274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65137254-A-G

38878274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65137254-A-T

http://identifiers.org/hco/4/GRCh38#38878330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65137310-A-C

38878356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65137336-A-T

38878361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65137341-A-G

38878378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65137358-T-G

38878423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65137403-T-C

38878425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65137405-T-C

38878466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65137446-T-A

38878484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138005-G-A

http://identifiers.org/hco/4/GRCh38#38878496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65138018-C-A

38878496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138018-C-G

http://identifiers.org/hco/4/GRCh38#38878501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65138023-C-A

38878508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138030-G-A

38878508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138030-G-T

38878515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138037-A-T

38878516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138038-T-C

38878517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138039-T-A

38878517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138039-T-C

38878550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138072-G-A

38878550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138072-G-T

38878567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138095-G-A

38878567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138095-G-C

38878567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138095-G-T

38878571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138099-G-A

38878571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138099-G-T

http://identifiers.org/hco/4/GRCh38#38878578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65138106-C-A

38878578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138106-C-T

38878581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138109-A-G

38878757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138284-G-C

38878842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138368-C-T

38878939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138443-T-G

38879230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138791-G-C

38879236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138797-G-T

38879250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138808-T-C

38879254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65138812-G-T

http://identifiers.org/hco/4/GRCh38#38879574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65139116-C-A

38879602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65139150-C-T

38879779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65139507-A-G

38881368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65140440-C-T

38881421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65140492-A-G

http://identifiers.org/hco/4/GRCh38#38881630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65142648-C-A

38881630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65142648-C-T

38881631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65142649-G-A

38881650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65142668-C-G

http://identifiers.org/hco/4/GRCh38#38881679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65142697-C-A

38881725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65142760-A-G

38881745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65142780-G-A

38881790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65142819-G-A

38881792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65142821-A-G

38881926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65143018-T-C

38883121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65143925-G-T

http://identifiers.org/hco/4/GRCh38#38883549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65144681-A-C

http://identifiers.org/hco/4/GRCh38#38885642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65146430-C-A

38885792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65146579-G-A

38885884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65146671-A-G

38885884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65146671-A-T

38886506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147419-G-A

38887294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147824-G-A

38887429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147942-G-C

38887828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148334-A-T

38887942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148434-A-G

38888551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149204-T-C

http://identifiers.org/hco/4/GRCh38#38888710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65149345-C-A

38888918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65149739-T-C

38889144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65149966-T-C

38889172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65149994-C-G

38889184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65150005-A-T

38889256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150077-A-T

38889345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150165-A-G

38889518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65150299-G-A

38889518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65150299-G-C

http://identifiers.org/hco/4/GRCh38#38889970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65150842-A-C

38890006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65150866-C-T

38890011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65150871-G-A

38890576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65151076-A-G

38890596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65151096-C-T

38890822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65151303-G-A

http://identifiers.org/hco/4/GRCh38#38891116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65152506-A-C

38891116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152506-A-G

38891134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152517-T-C

38891201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152596-C-T

38891274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152669-C-T

38891410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152802-C-G

38891436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152854-T-G

38891454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152879-C-T

38891470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152895-A-G

38891617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153020-T-A

38891633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153036-G-A

38891633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153036-G-T

38891666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153075-T-A

38891666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153075-T-G

38891667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153076-G-T

http://identifiers.org/hco/4/GRCh38#38891671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65153080-C-A

38891674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153083-A-T

38891697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153112-G-T

38891699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153114-G-A

http://identifiers.org/hco/4/GRCh38#38891726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65153141-A-C

38891726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153141-A-T

38891736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65153151-T-C

38891743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 65153158-G-A

38891743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 65153158-G-T

38891757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65153172-T-A

38891842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153257-A-G

38891878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153287-T-C

http://identifiers.org/hco/4/GRCh38#38891922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65153330-C-A

38891922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153330-C-T

38891929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153337-C-T

38891976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153380-A-G

38891988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153392-C-T

38892058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153462-T-A

http://identifiers.org/hco/4/GRCh38#38892092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65153495-A-C

38894251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65154007-G-T

38896714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155341-C-G

38896737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155365-C-T

38896952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155574-G-C

38897088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155699-A-G

38897110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155721-G-C

38897445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156257-G-T

38898024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156572-T-C

38898243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156747-G-C

38898473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156948-G-A

38898687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65157800-T-C

38898721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65157836-A-G

http://identifiers.org/hco/4/GRCh38#38898886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65158002-C-A

38901791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159403-G-A

38901932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159553-G-A

http://identifiers.org/hco/4/GRCh38#38902145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65159730-A-C

38902147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159732-T-C

38902192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159777-C-T

38902227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159811-A-G

38902298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159857-T-C

38902479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160003-A-G

38902489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160013-A-G

38902557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160074-A-G

38903059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160602-T-C

38903082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160621-C-G

38903145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160676-C-T

38903569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161184-A-G

38903873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161502-C-G

38904095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161977-T-C

38904095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161977-T-G

38904126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161995-T-G

38904259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65162119-G-A

http://identifiers.org/hco/4/GRCh38#38904342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65162195-A-C

38904342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65162195-A-G

38904366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65162219-A-T

38904619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65162428-G-A

38905005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65162700-A-G

38905160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65162827-G-A

38905191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65162831-G-C

38905513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163131-T-C

38905586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65163205-T-C

38905595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65163214-T-C

38905616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65163235-T-C

38905721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163339-G-A

38905950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163567-G-T

38906249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163849-C-T

38906367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163932-C-T

38906869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164195-C-G

38906869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164195-C-T

38906870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164196-G-A

38906870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164196-G-C

38906941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164249-C-T

38907242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164496-G-A

38907242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164496-G-T

38907626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165445-A-G

38907634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165456-G-A

38907651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165473-G-A

38907726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165552-A-G

38907773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165587-A-G

38908078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165869-A-G

38908189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165981-G-T

38908387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166125-T-C

http://identifiers.org/hco/4/GRCh38#38908461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65166199-C-A

38908461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166199-C-T

38908707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65166446-G-A

38908707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65166446-G-C

38908731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166470-G-A

38908766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166511-T-C

38908858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166555-C-T

38908870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166567-T-C

38908870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166567-T-G

http://identifiers.org/hco/4/GRCh38#38908872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65166569-C-A

38908872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166569-C-G

38908872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166569-C-T

38909119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166777-A-G

38909160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166819-A-G

38909229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166885-T-A

http://identifiers.org/hco/4/GRCh38#38911464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65168335-A-C

38911655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65168493-G-A

38913001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65169503-G-A

38913041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65169543-A-G

38913080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65169583-A-G

38913255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65169760-T-C

38914797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172543-T-C

38914836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172577-G-A

38914836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172577-G-T

http://identifiers.org/hco/4/GRCh38#38914839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65172580-C-A

38914839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172580-C-T

http://identifiers.org/hco/4/GRCh38#38914853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65172594-C-A

38914853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172594-C-G

38914853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172594-C-T

http://identifiers.org/hco/4/GRCh38#38915106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65172850-C-A

38915139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65172889-T-C

38915139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65172889-T-G

http://identifiers.org/hco/4/GRCh38#38915198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65172939-C-A

38915198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65172939-C-T

38915557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65173261-A-G

38918289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175063-C-T

38918343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175115-T-C

38919348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176360-C-G

38919640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176589-C-T

38919890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176960-C-T

38920891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177265-C-T

http://identifiers.org/hco/4/GRCh38#38921012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65177376-C-A

38921095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177452-C-T

38921752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177768-T-C

38921907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178114-T-A

38921907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178114-T-G

38921911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178118-T-C

38922670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178821-A-G

38922670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178821-A-T

http://identifiers.org/hco/4/GRCh38#38922677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65178828-A-C

38922677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178828-A-G

http://identifiers.org/hco/4/GRCh38#38922686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65178840-C-A

38922686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178840-C-T

38922757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178910-T-C

http://identifiers.org/hco/4/GRCh38#38922939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65179112-C-A

http://identifiers.org/hco/4/GRCh38#38922952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65179124-C-A

38922952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65179124-C-T

38923026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65179203-T-A

http://identifiers.org/hco/4/GRCh38#38923071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65179247-C-A

38923183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65179348-T-C

38923873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65180410-G-A

38923877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65180414-G-C

38923877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65180414-G-T

http://identifiers.org/hco/4/GRCh38#38924013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65180554-A-C

38924643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181169-G-A

38924693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181221-C-T

38924805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181329-G-A

38925054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182188-T-A

38925155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182302-T-G

38925325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182507-A-G

38925354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182535-A-G

38925354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182535-A-T

38925376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182560-G-A

38925518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182691-A-G

http://identifiers.org/hco/4/GRCh38#38925672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65182844-A-C

38925850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183016-A-T

38925865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183025-C-G

38925865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183025-C-T

38926124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183356-G-T

38926283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183475-G-C

38926283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183475-G-T

38926393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183527-A-G

38926863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65183682-C-T

38927180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65184107-A-G

38927381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65184373-G-A

http://identifiers.org/hco/4/GRCh38#38927401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65184393-C-A

38927463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65184453-T-C

38928703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185226-G-C

38928838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185378-G-A

38928981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185487-G-A

38928981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185487-G-T

38929055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185558-G-A

38929055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185558-G-C

38929055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185558-G-T

38929087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185588-A-G

38929095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185596-A-T

38929129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65185634-T-C

38929169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65185672-A-G

38929213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65185720-A-G

38929215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65185722-G-A

38929215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65185722-G-T

38929309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65185820-G-A

http://identifiers.org/hco/4/GRCh38#38929315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65185826-A-C

38929315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65185826-A-G

http://identifiers.org/hco/4/GRCh38#38929336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65185847-C-A

38929336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185847-C-T

38929384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185896-G-A

38929384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185896-G-C

38929384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185896-G-T

http://identifiers.org/hco/4/GRCh38#38929414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65185926-C-A

38929414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185926-C-G

38929414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185926-C-T

38929824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186026-A-G

38930004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186164-C-T

38930009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186169-A-G

38930038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186199-C-T

38930162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186313-C-T

38930210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186358-G-A

38930249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186398-T-C

38930394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186553-A-G

38930609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186723-G-T

38930726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186838-C-G

http://identifiers.org/hco/4/GRCh38#38930779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65186888-A-C

38930835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186949-C-T

38930843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186957-G-A

38930843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186957-G-T

38930918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65186994-C-G

38931034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187111-G-T

http://identifiers.org/hco/4/GRCh38#38931324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65187320-C-A

38931324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187320-C-T

http://identifiers.org/hco/4/GRCh38#38931330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65187326-C-A

38931418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187372-A-G

38931426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187380-A-G

http://identifiers.org/hco/4/GRCh38#38931501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65187458-A-C

38931501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65187458-A-G

38931555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65187512-G-T

38931561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65187518-T-G

http://identifiers.org/hco/4/GRCh38#38931567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65187524-C-A

38931567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65187524-C-T

38931585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65187542-G-C

38931693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187639-A-G

http://identifiers.org/hco/4/GRCh38#38931696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65187642-C-A

38931696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187642-C-T

http://identifiers.org/hco/4/GRCh38#38931697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65187643-C-A

38931697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187643-C-T

38931862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187955-T-A

38931862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187955-T-G

38931986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188087-G-A

38931993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188094-G-A

http://identifiers.org/hco/4/GRCh38#38932031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65188132-C-A

38932031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188132-C-T

38932059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188160-C-T

38932176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188525-T-C

38932288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65188651-T-C

38933427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189477-T-C

38933609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189673-A-G

38934053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189985-C-T

38934174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190087-A-T

38934180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190093-G-C

38934185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190098-A-G

38934206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190119-A-G

38934239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190154-A-G

38934275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190186-C-T

http://identifiers.org/hco/4/GRCh38#38934338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65190249-C-A

38934392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190302-T-C

38934773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190969-T-A

38934812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190993-C-G

http://identifiers.org/hco/4/GRCh38#38934865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65191045-A-C

38935284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191323-C-T

38935319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191354-G-T

38935396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191428-A-G

38935470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191502-T-A

38935583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191585-T-C

38935583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191585-T-G

http://identifiers.org/hco/4/GRCh38#38935586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65191588-C-A

38935586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191588-C-T

38935595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191597-A-G

http://identifiers.org/hco/4/GRCh38#38935604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65191606-C-A

http://identifiers.org/hco/4/GRCh38#38935654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65191647-C-A

38935654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191647-C-T

38935655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191648-G-A

38935655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191648-G-C

38935655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191648-G-T

http://identifiers.org/hco/4/GRCh38#38935687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65191678-C-A

38935687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191678-C-T

38935689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191680-T-C

38935706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191703-T-C

38935706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191703-T-G

38935718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 65191715-A-G

38935718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 65191715-A-T

38935746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65191743-G-T

38935810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191807-T-C

38935876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191871-T-A

38935904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191897-G-A

38935904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191897-G-T

http://identifiers.org/hco/4/GRCh38#38935924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65191918-C-A

38936045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192067-T-C

38936046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192068-A-T

38936436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192120-A-T

38937693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192993-G-A

38938161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193276-G-T

38938244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193358-G-A

38938333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193409-T-C

http://identifiers.org/hco/4/GRCh38#38938425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65193499-C-A

http://identifiers.org/hco/4/GRCh38#38938426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65193500-C-A

38938452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193509-G-A

38938452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193509-G-T

http://identifiers.org/hco/4/GRCh38#38938628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65193689-C-A

38938628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65193689-C-T

38938909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65193930-A-G

38938959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65193977-A-G

38939085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194099-C-T

38939203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194219-A-G

38939248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194264-G-C

38939546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65194553-T-C

38939584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65194603-T-A

38940382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195041-G-A

38940718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195815-G-T

38940823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195918-G-A

38940823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195918-G-T

38940875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195946-G-T

http://identifiers.org/hco/4/GRCh38#38940892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65195962-A-C

38940892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195962-A-T

http://identifiers.org/hco/4/GRCh38#38940908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65195978-C-A

38940908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195978-C-G

38940908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65195978-C-T

http://identifiers.org/hco/4/GRCh38#38941030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65196093-C-A

38941064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196124-A-T

http://identifiers.org/hco/4/GRCh38#38941126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65196189-C-A

38941126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196189-C-T

38941225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196331-G-A

38941343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196455-G-A

38941566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196671-C-G

38941566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196671-C-T

38941657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196764-A-T

38942277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65196950-A-G

38942876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197462-C-G

38943265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197549-T-C

38943307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197591-T-G

http://identifiers.org/hco/4/GRCh38#38943311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65197595-C-A

38943311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197595-C-T

38943316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197600-G-A

38943316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197600-G-T

http://identifiers.org/hco/4/GRCh38#38943335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65197848-C-A

38943335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197848-C-T

http://identifiers.org/hco/4/GRCh38#38943336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65197849-A-C

38943336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197849-A-G

http://identifiers.org/hco/4/GRCh38#38943342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65197855-A-C

38943342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197855-A-G

38943349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197862-T-A

38943349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197862-T-C

38943383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197898-T-C

38943383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65197898-T-G

38943570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198076-C-G

http://identifiers.org/hco/4/GRCh38#38943608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65198109-A-C

38943608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198109-A-G

38943842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198321-G-A

38943842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198321-G-C

38943842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198321-G-T

http://identifiers.org/hco/4/GRCh38#38943973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65198453-C-A

38943973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198453-C-T

http://identifiers.org/hco/4/GRCh38#38944015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65198495-C-A

38945113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198667-A-G

38945296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198830-A-G

38945365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65198894-T-C

http://identifiers.org/hco/4/GRCh38#38945433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65198962-C-A

38945735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25087
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65199240-C-G