64855851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103342792-T-G

64855866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103342807-T-C

64855953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103342890-T-A

64855953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103342890-T-C

http://identifiers.org/hco/17/GRCh38#64855959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103342896-C-A

64855961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103342898-T-C

64858698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103431581-T-C

64858714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103431597-T-C

64858769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103431652-T-C

64858868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103431751-G-A

64859302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432467-G-A

64859302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432467-G-T

64859305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432470-A-G

64859305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432470-A-T

64859338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432508-G-A

64859338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432508-G-T

64859339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432509-A-G

64859340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432510-T-C

64859340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432510-T-G

http://identifiers.org/hco/17/GRCh38#64859351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103432521-C-A

64859351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432521-C-T

64859389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432546-G-A

64859389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432546-G-T

http://identifiers.org/hco/17/GRCh38#64859409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103432560-A-C

64859409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432560-A-G

64859409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432560-A-T

64859415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432566-G-A

64859415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432566-G-C

64859415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432566-G-T

64859419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432570-T-A

64859419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103432570-T-C

64859481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432635-G-A

64859481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103432635-G-T

64859583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432737-T-G

64859616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432770-C-T

64859619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432773-A-G

64859620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103432774-T-G

64859623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103432777-G-T

64859703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432857-C-T

64859772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432926-G-C

64859784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432938-C-G

64859784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103432938-C-T

http://identifiers.org/hco/17/GRCh38#64859796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103432950-C-A

http://identifiers.org/hco/17/GRCh38#64859812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103432966-C-A

64859812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 103432966-C-T

64859888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433048-T-C

64859903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433063-C-T

64859931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433091-G-A

64859991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433151-G-C

http://identifiers.org/hco/17/GRCh38#64859996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#103433156-C-A

http://identifiers.org/hco/17/GRCh38#64860075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103433235-C-A

64860075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433235-C-G

64860075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433235-C-T

64860086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433246-G-C

64860272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433375-T-A

64860345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433448-C-T

http://identifiers.org/hco/17/GRCh38#64860356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103433459-C-A

64860356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433459-C-T

64860409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433506-G-A

64860409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433506-G-C

64860426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433523-C-T

64860467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433564-C-G

64860467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433564-C-T

64860492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433589-G-A

64860494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433591-G-A

64860506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433603-G-T

64860528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433625-G-A

64860528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103433625-G-C

64860628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433725-C-T

64860638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433735-C-G

64860667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433764-T-G

64860709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103433843-G-A

64860818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103434182-T-C

64861011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434378-T-A

64861031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434399-G-T

64861034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434402-C-T

64861133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434501-G-A

64861544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434872-C-T

64861629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434953-G-A

64861693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435012-T-C

64861719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435038-T-C

64861968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435275-A-G

64862490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103436223-C-T

64862522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103436253-A-G

64862626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103436357-G-A

64862963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103436647-C-T

http://identifiers.org/hco/17/GRCh38#64863032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103436716-C-A

http://identifiers.org/hco/17/GRCh38#64863096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103436764-C-A

64863096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103436764-C-T

64863117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103436786-T-G

64863181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103436876-A-G

64863184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103436879-G-T

64863197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103436892-G-A

64863197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103436892-G-T

http://identifiers.org/hco/17/GRCh38#64863215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103352416-A-C

64863215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103352416-A-G

64863240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103352439-T-C

64863280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103352464-G-A

64863280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103352464-G-C

64863280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103352464-G-T

64863377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103352545-T-G

64863379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103352547-C-T

64868502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103473487-G-A

64868674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103473649-A-T

64869177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475732-G-A

64869277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358492-G-A

64869277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358492-G-C

http://identifiers.org/hco/17/GRCh38#64869318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103358533-A-C

64869461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358669-T-C

64869554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358750-A-G

64869554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358750-A-T

64869556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358752-A-G

64869556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358752-A-T

http://identifiers.org/hco/17/GRCh38#64869560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103358756-A-C

64869560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358756-A-G

64869560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358756-A-T

64869690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103358864-A-G

64881102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103483867-A-T

64881106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103483871-A-G

http://identifiers.org/hco/17/GRCh38#64881162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103483931-C-A

64881753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484158-T-C

64881755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484160-A-T

64881840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484225-T-A

64881878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484262-C-G

64881987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484300-G-A

64881987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484300-G-T

64881997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484310-C-T

http://identifiers.org/hco/17/GRCh38#64882052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103484363-C-A

64882052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484363-C-T

64882366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103492096-C-T

64882709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103492431-A-G

64882722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103492444-C-T

64882830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103492566-T-C

64883504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493094-C-T

64883553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493142-A-G

64883609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493187-G-A

64883619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103493197-G-A

http://identifiers.org/hco/17/GRCh38#64883646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103493222-C-A

http://identifiers.org/hco/17/GRCh38#64883651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103493228-A-C

64883836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380416-G-C

64883995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380565-A-T

64886030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381870-A-G

http://identifiers.org/hco/17/GRCh38#64888755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103498078-C-A

64889220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499018-A-G

64891628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500060-G-A

64891923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500323-G-A

64892429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103500628-G-A

64892429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103500628-G-T

http://identifiers.org/hco/17/GRCh38#64892451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103500650-C-A

64892451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103500650-C-T

64892812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103501010-T-C

64892974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103501165-T-C

http://identifiers.org/hco/17/GRCh38#64893454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103502977-C-A

64893454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103502977-C-T

64894771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103503825-G-A

http://identifiers.org/hco/17/GRCh38#64894922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103508272-C-A

64894922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103508272-C-T

64894941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103508294-T-C

64895094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103508543-C-T

64895717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103510258-G-A

64895861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103393214-G-A

64895861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 103393214-G-C

64895861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 103393214-G-T

64895864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103393217-G-A

64895864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 103393217-G-C

64895864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 103393217-G-T

64895870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103393223-G-A

64895870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103393223-G-T

http://identifiers.org/hco/17/GRCh38#64895936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103510402-C-A

64895936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103510402-C-T

64895937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103510403-G-A

64895937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103510403-G-C

64895937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103510403-G-T

64895945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103510411-G-C

64895945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103510411-G-T

64895948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103510414-T-C

64895981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103510441-C-G

64896107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103510972-C-G

64896107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103510972-C-T

64896181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103511049-C-T

64896227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511095-A-G

64896227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511095-A-T

64896236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511104-T-C

64896255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511123-G-A

64896255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511123-G-C

64896255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511123-G-T

64896296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511173-G-A

64896296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511173-G-C

64896381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103511381-G-T

64896643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103511544-C-T

64896800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103511692-T-C

64896846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103511843-T-C

64896853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103511850-G-A

64896873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103511870-A-G

64897099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103512090-G-A

64897099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103512090-G-T

http://identifiers.org/hco/17/GRCh38#64897149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103512140-C-A

64897149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103512140-C-T

64897151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103512142-T-C

64897159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103512150-T-A

64897159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103512150-T-G

64902752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103514526-C-T

64902930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103514700-A-G

64904604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515124-A-G

64905219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515258-G-T

64905238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515277-T-C

64905259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515292-T-C

64905318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515341-A-G

64905318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103515341-A-T

http://identifiers.org/hco/17/GRCh38#64905396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103515423-C-A

64905396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103515423-C-G

64905396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103515423-C-T

http://identifiers.org/hco/17/GRCh38#64906208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103516554-C-A

64908195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518023-G-T

64908354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518156-T-C