64586780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3 prime UTR variant
orthologous variants: 18114726-T-C

64587353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3 prime UTR variant
orthologous variants: 18115158-G-A

64587537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3 prime UTR variant
orthologous variants: 18115336-T-C

64587646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3 prime UTR variant
orthologous variants: 18115457-T-A

64587646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3 prime UTR variant
orthologous variants: 18115457-T-G

64587667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3 prime UTR variant
orthologous variants: 18115483-A-G

64587710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: synonymous variant
orthologous variants: 18115525-A-G

64588363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18116169-C-T

64588636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18116440-A-G

64588901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18116697-C-G

64589363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18117122-C-G

http://identifiers.org/hco/8/GRCh38#64589769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18117154-C-A

64589803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 18117188-T-C

64589871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18117261-A-G

64590447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18117805-C-T

64590517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18117880-T-C

64590692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18118041-G-A

64590705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18118054-A-T

64590884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18118376-G-A

http://identifiers.org/hco/8/GRCh38#64591463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18118920-A-C

64591472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18118928-T-C

64591582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119033-A-G

64591591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119042-G-A

64591656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119104-T-C

64591678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119125-G-A

64591735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119182-A-G

64591889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119308-T-C

64591904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119323-G-T

64592276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119621-A-G

64592379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119726-G-C

64592413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119767-T-A

64592451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119805-T-C

64592483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18119837-C-G

64595357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18125520-C-T

64595711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18125736-C-T

64595905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18125918-C-T

64595957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18125970-C-T

64595963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18125976-A-G

64596020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126033-T-C

64596101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126113-T-C

64596103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126115-T-A

http://identifiers.org/hco/8/GRCh38#64596143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18126155-A-C

64596143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126155-A-G

http://identifiers.org/hco/8/GRCh38#64596187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18126199-C-A

64596203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126214-T-C

64596358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126361-T-C

http://identifiers.org/hco/8/GRCh38#64596492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18126483-A-C

64596514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126504-G-T

http://identifiers.org/hco/8/GRCh38#64596533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18126523-C-A

64596533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126523-C-T

http://identifiers.org/hco/8/GRCh38#64596564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18126554-A-C

64596564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126554-A-T

64596583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18126571-A-T

64596675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126663-A-G

64596681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126669-T-G

64596693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126681-A-T

64596714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126702-G-A

64596714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18126702-G-C

64596717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126705-T-C

64596720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126708-T-C

64596782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 18126770-G-A

64596782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18126770-G-C

64596792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18126780-C-T

64596862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18126850-T-A

64596867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126855-C-T

64596884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18126872-T-C

64596886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18126874-G-C

64596918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 18126906-A-G

64597163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18127108-C-T

64597267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18127613-C-T

http://identifiers.org/hco/8/GRCh38#64597502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18127819-C-A

http://identifiers.org/hco/8/GRCh38#64597699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18128058-C-A

64597834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18128209-T-C

64598028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18128395-T-C

64598052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18128419-A-G

64598389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18128772-C-T

64598397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18128780-C-T

64598542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18130698-C-T

64598624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18130782-G-T

64598633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18130792-T-C

64599719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18131331-G-A

64600015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18131558-G-A

64600053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18131592-G-C

64600178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18131716-T-C

64600180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18131718-G-T

64600181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18131719-T-C

64600181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18131719-T-G

64603340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132097-C-T

64603586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132337-A-T

64603621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132372-C-T

http://identifiers.org/hco/8/GRCh38#64603720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18132456-C-A

64603720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132456-C-T

64603906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132647-A-T

64603968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132704-C-T

64603989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132725-A-G

64604142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18132879-C-T

64604265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133004-C-G

64604460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133099-C-T

64604516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133160-C-T

64604535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133179-G-T

64604616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133302-G-A

64604616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133302-G-C

64604665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133452-G-T

64604673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133460-T-A

http://identifiers.org/hco/8/GRCh38#64604720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18133507-C-A

64604720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18133507-C-G

64604748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18133535-C-T

64604786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18133573-T-C

64604882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133665-C-G

http://identifiers.org/hco/8/GRCh38#64604885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18133668-A-C

64605059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18133834-T-G

64605386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18134124-G-A

64605855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18134590-G-C

64605912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18134647-T-C

64606034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18134767-T-C

64606216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18134949-T-G

http://identifiers.org/hco/8/GRCh38#64606318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18135051-C-A

64606329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18135062-G-A

64607078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18135806-C-T

64608135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18136879-C-T

64608306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18137020-T-A

64608405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18137119-G-A

64608736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18137404-G-A

64608952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18137646-C-T

64609064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18137757-T-C

http://identifiers.org/hco/8/GRCh38#64609076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18137769-A-C

64609076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18137769-A-G

64609124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18137815-A-G

64609500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18138854-T-C

64609500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18138854-T-G

64609644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18139071-G-A

64609665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18139095-T-A

64609667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18139097-C-G

64609705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18139139-G-A

64609705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18139139-G-C

64609707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18139141-T-C

http://identifiers.org/hco/8/GRCh38#64609760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18139199-C-A

64609760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18139199-C-T

http://identifiers.org/hco/8/GRCh38#64610717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18140027-C-A

64610732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18140039-G-A

64610742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18140049-T-C

64610747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18140054-A-G

64610885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18140173-G-A

64611366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18140669-G-A

64611514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18140818-A-G

64613277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18147537-A-G

64613353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18148016-T-C

64613698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18148367-T-A

64614093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18149747-A-T

64614198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18149840-T-C

64614208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18149850-C-T

64614467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18150117-C-T

http://identifiers.org/hco/8/GRCh38#64614676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18150330-A-C

64614676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18150330-A-G

64614676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18150330-A-T

64614726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18150382-G-C

64614744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18150400-A-G

64614761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18150417-T-C

64615004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18150665-A-G

64615154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18150815-C-T

http://identifiers.org/hco/8/GRCh38#64615356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18151017-C-A

64615423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18151092-G-T

http://identifiers.org/hco/8/GRCh38#64615512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18151183-A-C

64615614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18151291-G-A

64615614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18151291-G-T

64615627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18151304-T-C

64615707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18151384-C-T

http://identifiers.org/hco/8/GRCh38#64615829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18151506-C-A

64615829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18151506-C-G

64615841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18151518-G-A

64615890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18151567-T-A

64616129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18151806-G-A

64616129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18151806-G-T

64616168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18151845-T-C

64616193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: synonymous variant
orthologous variants: 18151870-A-G

http://identifiers.org/hco/8/GRCh38#64616342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18152008-A-C

64616392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152067-A-G

64617494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152323-A-G

64617630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152456-C-T

64617996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152830-G-T

64618000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152834-G-A

64618101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152946-A-G

64618102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152947-G-T

64618129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152972-A-G

64618129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18152972-A-T

64618318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153158-G-C

64618372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153212-G-A

64618404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153242-A-T

http://identifiers.org/hco/8/GRCh38#64618415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18153253-C-A

64618533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153373-G-T

64618592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153430-C-T

64618596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153434-C-T

64618615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153448-C-T

64618672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153478-T-C

64618673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18153479-G-A

64618948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18154181-C-T

64619338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18154566-T-C

64619552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18154777-T-A

http://identifiers.org/hco/8/GRCh38#64619714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18154901-A-C

64619722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18154909-G-T

64620480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18155376-T-C

64620499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18155395-A-G

http://identifiers.org/hco/8/GRCh38#64624273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18157746-A-C

64624273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157746-A-T

64624279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157751-G-A

64624279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157751-G-T

64624311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157773-T-C

64624311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157773-T-G

64624356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157818-G-C

64624356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157818-G-T

64624389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18157851-G-A

http://identifiers.org/hco/8/GRCh38#64624390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18157852-A-C

64624491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: synonymous variant
orthologous variants: 18157953-T-A

64624606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18158030-T-G

64624635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18158056-T-G

64624685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18158104-T-C

64624688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18158107-T-A

64625374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18158245-G-A

64625374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18158245-G-C

64625411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18158282-G-C

64625713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18159190-G-A

64625916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18159344-T-C

64626353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18159773-T-C

http://identifiers.org/hco/8/GRCh38#64626442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18159855-A-C

64626511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18160047-T-C

64626911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18160411-A-G

64627345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18161431-T-C

64627602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18161668-T-C

64627692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18161756-T-A

64627712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18161776-G-A

http://identifiers.org/hco/8/GRCh38#64627800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18161864-A-C

64628011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18162058-G-A

64628017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18162064-G-A

64628028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18162075-G-C

64628850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18162480-C-T

64628863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18162493-T-C

64629272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18163230-A-G

http://identifiers.org/hco/8/GRCh38#64629775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18164699-C-A

64629917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18164786-T-C

64629917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18164786-T-G

64630446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18165262-T-C

64630851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18165606-T-A

64630851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18165606-T-C

http://identifiers.org/hco/8/GRCh38#64634044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18172665-C-A

64634224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18172823-T-C

64634680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18172923-A-G

64634723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18172963-G-C

64634738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18172980-G-A

64634745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18172987-A-G

64634937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18173138-G-A

http://identifiers.org/hco/8/GRCh38#64635177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18173373-C-A

64635527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18173687-C-T

64635791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18173928-C-T

http://identifiers.org/hco/8/GRCh38#64637198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18174688-C-A

64637202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18174692-A-G

64640085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18175184-G-T

http://identifiers.org/hco/8/GRCh38#64640104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18175201-C-A

http://identifiers.org/hco/8/GRCh38#64640163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18175250-A-C

64640582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18175932-G-T

64640625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18175975-T-C

64640760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18177251-C-T

64641013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18177501-G-C

64641013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18177501-G-T

64641062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18177550-A-G

64641480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18177935-G-C

64641930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18178292-G-A

64660911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18179755-A-G

64661100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18179910-G-A

64661282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18180080-G-A

64661388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18180194-C-T

64663356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181342-C-T

64663423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181408-C-T

64663451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181435-T-A

http://identifiers.org/hco/8/GRCh38#64663472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18181450-C-A

64663493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181471-T-G

64663617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181547-T-C

64663656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181585-G-C

64663656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181585-G-T

http://identifiers.org/hco/8/GRCh38#64663721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18181685-C-A

64663776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181726-T-G

64663778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18181728-T-A

64664190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18182022-C-T

http://identifiers.org/hco/8/GRCh38#64664257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18182116-C-A

64666739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18183907-G-A

64666750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18183918-T-A

64666809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18183960-G-A

64666880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18184033-G-A

64667024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18184167-A-G

64667463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18185971-T-C

64667500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18186013-A-G

64667715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18186199-T-G

64667778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18186264-G-C

64668026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18186474-C-T

64668034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18186482-G-C

64668101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18186630-G-T

64668750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18187268-G-A

http://identifiers.org/hco/8/GRCh38#64668797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18187314-A-C

64668825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18187342-A-G

64668924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18187442-T-C

64669209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18187648-G-T

64669282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18187717-C-T

64669428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18187849-G-A

64669463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18187881-G-A

64670136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18188421-C-T

64670293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18188562-T-C

64670418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18188696-A-G

64670498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18188728-T-C

64671614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18190703-C-T

64672016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18191071-A-G

64672048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18191096-A-T

64672100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18191148-T-C

64672255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18191300-C-T

64673224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18192397-G-A

64673367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18192519-A-G

64673502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18192652-C-T

64673677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18192826-C-T

64674227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18193362-A-G

64674548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18193666-G-C

64674910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18194081-T-C

64674920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18194091-A-G

http://identifiers.org/hco/8/GRCh38#64675323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18197373-C-A

64675487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18197530-T-C

64675740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18197786-G-A

64675757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18197803-G-A

64675791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18197854-A-G

64675815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18197878-T-C

64675979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18198023-C-G

64676258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18198282-G-C

http://identifiers.org/hco/8/GRCh38#64676345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18198360-C-A

64676345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18198360-C-T

http://identifiers.org/hco/8/GRCh38#64676381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18198395-C-A

64677097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18199108-C-T

64677338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18199336-G-A

64677479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18199449-T-A

64677790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18199741-T-C

64678104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18200182-C-T

http://identifiers.org/hco/8/GRCh38#64678386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18200432-C-A

64679025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18201046-C-T

64679161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18201175-C-G

64679347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18201380-T-C

64679349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18201382-G-T

64680501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18202595-T-C

64687397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18204748-G-A

64687760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205024-C-T

64687778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205037-G-A

64687964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205230-T-G

64688031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205330-A-G

http://identifiers.org/hco/8/GRCh38#64688052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18205351-C-A

64688177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205470-G-A

64688238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205501-T-C

http://identifiers.org/hco/8/GRCh38#64688392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18205594-C-A

64688392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205594-C-G

64688989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205832-T-C

64689080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205917-A-G

64689123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18205962-C-T

64689408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18206242-T-C

http://identifiers.org/hco/8/GRCh38#64689412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18206246-C-A

64689517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18206337-G-C

64689517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18206337-G-T

64690813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207321-A-G

64690820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207328-T-A

64690828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207336-C-T

64690882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207391-G-C

64690988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207479-T-C

64691011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207502-T-C

64691023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207514-C-T

64691091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207582-T-C

64691099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207590-G-C

64691292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207737-T-C

64691522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207876-C-G

64691567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207915-C-T

64691598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18207948-G-A

64691949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 18208483-T-C

64692019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 18208562-G-A

64692019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 18208562-G-T

64692109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 18208628-C-T

64692137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 18208654-C-T

64692160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, missense_variant
orthologous variants: 18208671-T-G

64692203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, start_lost
orthologous variants: 18208711-C-T

64692280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18208775-T-G

64692472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18208971-A-G

64692626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18209105-T-C

64692820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18209312-T-A

64692845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18209340-C-T

64692868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18209362-A-G

64693309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18209775-G-A

64693507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18209972-T-G

64693553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18210010-A-G

64693607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18210050-A-G

64693719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18210156-C-T

64693900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18210313-G-C

http://identifiers.org/hco/8/GRCh38#64693944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18210354-C-A

64693944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18210354-C-T

http://identifiers.org/hco/8/GRCh38#64694120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18210518-C-A

64694151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18210548-G-T

64694711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18211794-T-C

64694819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18211916-T-C

64694927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18212025-T-C

64694991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212097-G-A

64695002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18212103-A-G

64695009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18212110-A-G

64695053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18212148-T-A

http://identifiers.org/hco/8/GRCh38#64695178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#18212262-A-C

64695201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212285-C-T

64695334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212414-A-G

http://identifiers.org/hco/8/GRCh38#64695433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18212493-C-A

64695433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18212493-C-G

64695664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212697-A-T

64695713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212738-G-A

64695713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212738-G-T

64695745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212771-T-A

64695745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212771-T-C

64695824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18212847-T-A

64696394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18213238-G-A

64696685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18213513-T-C

64696714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18213539-G-A

64697001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18213829-C-T

64697197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18214026-T-C

64697220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18214052-C-T

64697830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18214641-C-T

64697931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18214725-G-A

64697940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18214733-T-C

64698895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18215680-T-C

http://identifiers.org/hco/8/GRCh38#64698898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18215683-A-C

64698898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18215683-A-G

64699160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18215944-C-T

64699344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18216128-T-A

http://identifiers.org/hco/8/GRCh38#64699869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18216670-A-C

64700035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18216831-T-C

64700045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18216841-G-C

64700109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18216897-G-A

64700163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18216955-A-G

64700974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18217736-T-C

64702216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18218981-C-T

http://identifiers.org/hco/8/GRCh38#64702753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18219519-C-A

64702753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18219519-C-T

64703203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18219964-T-C

64703352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18220104-C-T

http://identifiers.org/hco/8/GRCh38#64703684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18220346-C-A

64703684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 18220346-C-T

64703842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18220507-C-T

64703858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18220526-A-G

64703866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18220534-A-G

64703914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18220582-T-C

64703988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18220647-T-C

64704326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18220953-A-G

64704364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18220980-T-C

64704526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18221148-A-T

64704730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18221383-C-T

64704865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18221519-T-C

64705133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18221922-A-G

64705202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18221993-G-A

64705202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18221993-G-T

64705468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18222247-G-A

http://identifiers.org/hco/8/GRCh38#64705729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18222567-A-C

http://identifiers.org/hco/8/GRCh38#64706037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18222875-C-A

64706201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18223394-C-G

64706434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18223614-T-C

64706455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18223638-T-C

64706705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18223863-G-A

64710980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18230827-T-C

64711065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18230917-T-C

64711147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18231007-T-C

64712259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18232738-G-A

64712259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18232738-G-C

64712288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18232758-T-A

http://identifiers.org/hco/8/GRCh38#64712499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18232955-A-C

64712573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233015-C-T

64712593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233034-C-T

64713041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233419-C-G

64713041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233419-C-T

64713134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233509-C-G

64713181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233548-T-C

64713186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233553-C-T

64713295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18233677-C-T

http://identifiers.org/hco/8/GRCh38#64713625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18233945-A-C

64713704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18234013-G-A

64714390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18234921-T-C

64714817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18235349-C-T

64714973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18235479-A-T

64717963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18239023-T-G

http://identifiers.org/hco/8/GRCh38#64718402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18239406-C-A

64718402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18239406-C-T

http://identifiers.org/hco/8/GRCh38#64718734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18239756-C-A

64718734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18239756-C-T

64718740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18239762-A-G

64718881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18239883-T-A

64718964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18239975-T-C

64718989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18240006-G-A

64719106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18240116-G-A

64719106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18240116-G-T

64719167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18240178-A-G

64719235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18240280-A-G

64719251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18240296-A-G

64719309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18240354-T-C

64720133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18241181-G-A

64720287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18241335-T-C

64720315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18241363-A-G

64720626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18241683-G-C

64720702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18241755-A-G

64720762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18242005-T-C

64720762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18242005-T-G

http://identifiers.org/hco/8/GRCh38#64721087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18242331-A-C

64721233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18242477-A-G

64721489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18242679-T-C

64721824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243165-T-A

64721824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243165-T-C

64721895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243235-A-G

64721904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243244-C-T

64722040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243377-C-T

64722252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243606-A-T

64722255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243609-G-T

64722324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243662-C-G

64722508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243810-T-G

64722547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243849-G-C

64722598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243896-A-G

64722598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243896-A-T

64722662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18243987-C-T

64722724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244053-G-A

64722742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244071-G-C

64722742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244071-G-T

64722745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244074-G-A

64722745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244074-G-C

64722745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244074-G-T

64722753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244082-G-A

64722753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244082-G-C

64722753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244082-G-T

64722755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244084-G-A

64722755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244084-G-C

64722755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244084-G-T

64722805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244128-G-C

64722805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244128-G-T

64722907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244230-C-T

64723183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244497-G-A

64723441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244785-G-C

64723569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18244948-T-C

64725528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246526-C-G

64725699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246649-A-G

64725819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246759-T-A

64725819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246759-T-C

64725945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246874-T-C

64725945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246874-T-G

64725998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246925-C-G

64725998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246925-C-T

64726010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246937-G-C

64726011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18246938-G-A

64726319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18247245-G-A

http://identifiers.org/hco/8/GRCh38#64726364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18247306-A-C

http://identifiers.org/hco/8/GRCh38#64726654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18247599-A-C

64726687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18247644-T-C

64727368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248308-A-G

64727422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18248357-A-G

64727482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248416-C-T

64727515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248449-T-C

64727515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248449-T-G

64727566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248498-G-A

64727618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248531-G-T

64727645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248558-A-G

64727688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248583-T-C

64727705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248600-G-A

64727852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18248767-A-G

64728026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18248937-G-T

64728032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18248943-T-C

64728122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18249033-C-T

64728135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18249046-G-A

64728135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18249046-G-T

64728217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18249129-T-C

64728473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18249390-T-A

64728546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18249459-G-A

64728666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18249557-T-C

64728701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18249580-A-G

http://identifiers.org/hco/8/GRCh38#64744555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18258978-A-C

64745192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18259618-T-C

64745732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18260162-A-G

64745876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18260306-G-C

64745876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18260306-G-T

64746554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18260881-G-A

64747017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18261271-G-A

64747017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18261271-G-T

http://identifiers.org/hco/8/GRCh38#64747068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18261308-A-C

64747111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18261343-T-C

64747943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18261604-G-A

64747958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18261619-C-G

http://identifiers.org/hco/8/GRCh38#64748153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18261811-A-C

64748332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18262006-T-C

http://identifiers.org/hco/8/GRCh38#64748598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18262267-C-A

http://identifiers.org/hco/8/GRCh38#64748625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18262290-C-A

64748630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18262295-C-T

64748691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18262349-A-T

64749879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18262995-C-T

64749961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18263053-C-T

64750048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18263138-G-C

64750238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18263354-G-A

64750929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18264453-C-T

64751003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18264576-C-T

64751015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18264588-C-T

64751052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18264711-A-G

http://identifiers.org/hco/8/GRCh38#64751275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18264957-C-A

64751430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18265103-C-T

64751596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18265272-G-A

64751632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18265308-G-T

64751919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18265723-G-A

64751995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18265783-T-C

64752216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18265987-T-C

64752365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18266133-A-T

http://identifiers.org/hco/8/GRCh38#64752395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18266182-C-A

64752395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18266182-C-T

64754931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18266944-A-T

64755129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18267111-G-A

64756380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18269186-A-G

64756781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18269545-C-G

64756832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18269592-A-G

64757115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18269843-G-C

64757174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18269901-G-C

64757413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18270098-T-C

64761626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18273338-T-G

64761657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18273369-C-T

64761856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18273563-G-A

64761862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18273569-G-A

64762019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18273722-C-T

64762774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18275331-C-T

64762807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18275364-T-C

64762808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18275365-A-G

64762943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18275489-A-G

64769744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18275895-C-T

64769779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18275930-C-T

64770189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18276408-A-G

64770710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18276886-A-T

http://identifiers.org/hco/8/GRCh38#64771643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18279016-C-A

64771737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18279101-C-T

64771786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18279153-C-T

64773381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18280039-G-T

64773405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18280063-C-T

64774210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18280529-T-C

64774423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18280709-T-C

64774755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18280959-C-T

64775830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18282335-T-C

64775843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18282347-T-C

64776178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18282835-G-T

64776374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18283023-A-T

64776465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18283114-G-A

http://identifiers.org/hco/8/GRCh38#64776651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18283229-C-A

64776672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18283238-T-C

64776744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18283271-G-C

64776940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18283382-T-G

http://identifiers.org/hco/8/GRCh38#64777156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18283576-C-A

http://identifiers.org/hco/8/GRCh38#64777532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18283979-C-A

64777532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18283979-C-G

64777535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18283982-G-A

64777874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18284379-T-C

64777911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18284409-A-T

64778053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18284545-T-C

64778054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18284546-T-C

64778157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18284648-G-T

64778164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18284655-A-G

http://identifiers.org/hco/8/GRCh38#64778344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18284805-C-A

64778941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18285395-A-G

64779457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18286316-A-G

64779680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18286480-G-T

64779737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18286535-G-T

http://identifiers.org/hco/8/GRCh38#64779878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18286678-C-A

64779882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18286682-G-A

64780183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18287105-G-A

64780900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18287787-G-A

64781156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18287985-T-C

http://identifiers.org/hco/8/GRCh38#64781313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18288116-A-C

64783047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18289443-A-G

64783059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18289455-C-T

64783077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18289478-C-T

64784232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18291281-C-T

64784577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18291835-G-A

64784585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18291843-G-A

64784636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18291895-G-C

64784756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18292013-A-G

64785057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18292337-C-T

64785099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18292382-T-C

64785210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18292474-T-G

64785373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18292629-T-C

http://identifiers.org/hco/8/GRCh38#64785421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18292677-C-A

64795787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18293907-T-C

64795854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18293979-G-A

64795884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18294019-A-T

64796152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18294398-G-A

http://identifiers.org/hco/8/GRCh38#64796255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18294968-C-A

http://identifiers.org/hco/8/GRCh38#64796538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18295537-C-A

64796672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18295621-A-G

64796778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18295695-T-C

64796923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18295829-G-T

64796942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18295857-G-C

64797118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18296061-G-C

64797141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18296085-T-C

64797141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18296085-T-G

64797425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18296329-T-C

64797747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18296607-A-G

64797812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18296667-T-C

64798236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297043-T-G

64798274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297078-T-C

http://identifiers.org/hco/8/GRCh38#64798397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18297196-C-A

64798397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297196-C-G

64798397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297196-C-T

http://identifiers.org/hco/8/GRCh38#64798403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18297201-C-A

64798403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297201-C-G

64798410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297208-G-A

64798410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297208-G-C

64798410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: intron variant
orthologous variants: 18297208-G-T

64798480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: synonymous variant
orthologous variants: 18297266-A-T

64798482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18297268-G-A

64798482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18297268-G-C

64798482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18297268-G-T

http://identifiers.org/hco/8/GRCh38#64798512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#18297298-C-A

64798512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18297298-C-T

64798518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18297304-G-A

64798518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18297304-G-C

64798518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: missense variant
orthologous variants: 18297304-G-T

http://identifiers.org/hco/8/GRCh38#64798698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#18297429-C-A

64798698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 18297429-C-G

64798698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2652
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 18297429-C-T