64784914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103257434-T-C

http://identifiers.org/hco/17/GRCh38#64784917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103257437-C-A

http://identifiers.org/hco/17/GRCh38#64784952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103257476-A-C

64784955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103257479-G-A

64784955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103257479-G-T

64785056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103257551-G-T

64785248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103257705-G-A

64785248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103257705-G-T

64785384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257837-A-T

64786023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258105-T-C

64786104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258185-G-A

64786501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258358-T-C

64786546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258402-C-T

64786731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103258587-A-G

64787169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103258851-C-T

http://identifiers.org/hco/17/GRCh38#64787225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103258913-C-A

64787225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103258913-C-T

64787239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103258925-C-T

64787278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103258964-C-G

64787278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103258964-C-T

http://identifiers.org/hco/17/GRCh38#64787289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103258975-A-C

64787289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103258975-A-G

64787289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103258975-A-T

64787331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259017-G-A

64787331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259017-G-T

64787368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103259062-G-A

64787368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103259062-G-T

64788533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259552-C-T

64790540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260326-T-C

http://identifiers.org/hco/17/GRCh38#64790762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103260485-C-A

64790893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260558-C-T

64791035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260710-G-A

64791318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260978-C-T

64791454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261105-C-T

64791503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261157-C-T

64791536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261187-C-T

http://identifiers.org/hco/17/GRCh38#64791539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103261189-C-A

64791648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261276-A-G

64791707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261333-G-A

64791802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261377-C-T

64792337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261676-G-A

64792337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261676-G-C

64792337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261676-G-T

64792483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103261822-C-G

64792483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103261822-C-T

64792495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103261834-G-T

64792525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103261864-C-T

64792558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261897-G-T

64792594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261919-C-T

64792805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262129-T-C

http://identifiers.org/hco/17/GRCh38#64794081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103262757-C-A

64794111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262784-G-A

64794184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262853-C-T

64794232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262884-G-A

64794340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262991-G-A

64794360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263011-C-T

64794514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263166-C-T

64794515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263167-G-A

http://identifiers.org/hco/17/GRCh38#64795223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

http://identifiers.org/hco/17/GRCh38#64797221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103264710-C-A

64797221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264710-C-T

64797222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264711-C-T

http://identifiers.org/hco/17/GRCh38#64797223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103264712-C-A

64797255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264757-G-A

64797255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264757-G-C

64797258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264760-A-T

64797661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265391-G-A

64797700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265428-T-G

64797814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265526-T-G

64798008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265705-C-T

64798143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265798-G-A

http://identifiers.org/hco/17/GRCh38#64798397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103266036-C-A

64798397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103266036-C-T

64798602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103266177-T-C

64799369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103266925-T-C

64799421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103266975-C-T

http://identifiers.org/hco/17/GRCh38#64799489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103267039-C-A

64799489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103267039-C-T

64799677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267188-A-T

64799767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267261-G-A

64799948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267372-G-A

64799948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267372-G-T

64799968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267388-A-G

64799969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267389-G-T

http://identifiers.org/hco/17/GRCh38#64800037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103267456-C-A

64800037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103267456-C-T

http://identifiers.org/hco/17/GRCh38#64800103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103267522-C-A

64800172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103267591-G-A

64800491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103267910-C-T

64800510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103267929-C-G

64800520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103267939-G-A

64800520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103267939-G-T

http://identifiers.org/hco/17/GRCh38#64800639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103268061-C-A

64800787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103268209-C-T

64800900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103268322-G-A

64800900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103268322-G-T

64800966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103268383-G-T

http://identifiers.org/hco/17/GRCh38#64800998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103268415-C-A

http://identifiers.org/hco/17/GRCh38#64801044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103268448-C-A

64801348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103268701-G-T

64802874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269149-C-T

64803028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269277-G-A

64803121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269374-T-C

64803525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

http://identifiers.org/hco/17/GRCh38#64803683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103269724-C-A

64803683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269724-C-T

64803785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269820-C-G

64803798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269838-G-A

64803798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269838-G-T

64804724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103270764-G-T

64804747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103270786-T-C

64804786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103270828-G-A

64804786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103270828-G-C

http://identifiers.org/hco/17/GRCh38#64804826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103270856-C-A

64804826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103270856-C-T

64804846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103270876-T-C

64804873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103270951-G-A

64804873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103270951-G-C

64804873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103270951-G-T

64804879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103270957-G-T

http://identifiers.org/hco/17/GRCh38#64804901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103270979-C-A

64804911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103270989-G-A

64804911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103270989-G-T

64805027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271105-T-G

64805036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271114-C-T

64805040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271118-T-C

64805041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271119-C-G

64805041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271119-C-T

64805046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271124-G-A

64805046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271124-G-C

64805046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271124-G-T

64805047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103271125-T-A

64805103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103271181-G-C

64805103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103271181-G-T

64808593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103272923-C-T

http://identifiers.org/hco/17/GRCh38#64808655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#103272980-C-A

http://identifiers.org/hco/17/GRCh38#64809084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103273405-C-A

64809084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273405-C-G

64809084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273405-C-T

http://identifiers.org/hco/17/GRCh38#64810343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103274203-A-C

64810843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103274578-C-T

64812419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103274943-A-G

64812581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103275127-T-G

64812589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103275136-G-A

http://identifiers.org/hco/17/GRCh38#64812636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103275185-A-C

64812811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275343-C-T

64814672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103277618-G-A

http://identifiers.org/hco/17/GRCh38#64814747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103277677-A-C

64814747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103277677-A-G

64814769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103277696-A-G

64814968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277880-A-G

64815012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277945-G-A

64815012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277945-G-C

64815012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277945-G-T

64815055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103277982-G-A

64815254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103278183-T-C

64815263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103278209-A-G

64815294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278240-T-A

64815294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278240-T-C

http://identifiers.org/hco/17/GRCh38#64815296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103278242-C-A

64815296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278242-C-T

64815308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278254-G-A

64815308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278254-G-T

64815333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278279-G-T

http://identifiers.org/hco/17/GRCh38#64815369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#103278304-A-C

http://identifiers.org/hco/17/GRCh38#64815372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103278307-A-C

64815383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278318-T-A

64815383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278318-T-C

64815383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278318-T-G

http://identifiers.org/hco/17/GRCh38#64815394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103278333-C-A

64815394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278333-C-G

64815394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278333-C-T

http://identifiers.org/hco/17/GRCh38#64815417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#103278357-C-A

64815487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278413-G-A

http://identifiers.org/hco/17/GRCh38#64815541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103278465-A-C

64816323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279138-T-C

64816325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279140-C-G

64816866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279576-G-A

64818899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283291-A-G

64818951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283341-A-G

64818972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283360-C-T

64819095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283484-A-G

64819268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283590-C-G

64821041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103284985-T-C

64821050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103284994-A-G

http://identifiers.org/hco/17/GRCh38#64821059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103285008-C-A

64821074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285028-A-G

http://identifiers.org/hco/17/GRCh38#64821086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103285045-C-A

64821086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285045-C-T

64821105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285064-A-G

64821141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285080-G-A

64821141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285080-G-T

64821161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285095-G-A

http://identifiers.org/hco/17/GRCh38#64821166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103285100-C-A

64821166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285100-C-T

64821265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285195-T-C

64821283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285212-T-G

64821713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103285501-G-A

64821795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103285542-C-T

64822438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286187-A-G

64822447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286196-T-A

64822447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286196-T-C

64822463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286212-T-G

64822494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286250-A-T

http://identifiers.org/hco/17/GRCh38#64823620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103286906-C-A

64823716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286996-A-G

http://identifiers.org/hco/17/GRCh38#64824509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103287755-C-A

64824509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103287755-C-G

64824560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103287803-A-G

64824570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103287813-T-C

64824605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103287834-C-T

http://identifiers.org/hco/17/GRCh38#64824622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103287850-C-A

64824622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103287850-C-T

64824944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103288172-T-C

http://identifiers.org/hco/17/GRCh38#64824961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103288189-A-C

64825026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103288244-T-C

64825052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103288263-A-G

64828018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103292878-A-G

64828055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103292905-C-T

64828188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293036-A-G

64828522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293302-T-C

64828565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293335-C-T

http://identifiers.org/hco/17/GRCh38#64828703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103293490-A-C

http://identifiers.org/hco/17/GRCh38#64829133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103294623-C-A

64829133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294623-C-T

http://identifiers.org/hco/17/GRCh38#64829152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103294642-C-A

64829152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294642-C-G

64829152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294642-C-T

http://identifiers.org/hco/17/GRCh38#64829197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103294684-C-A

64829197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: non coding transcript exon variant
orthologous variants: 103294684-C-T

64829520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35411
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294971-A-G