64718169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104982098-T-A

64718186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104982081-G-T

64718314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981971-A-G

64718329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981956-G-C

http://identifiers.org/hco/5/GRCh38#64718500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104981818-C-A

64718500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981818-C-T

64718509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981809-T-C

64718542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981757-T-A

64718594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981709-G-T

64718606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981697-C-T

64718727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104981035-T-C

http://identifiers.org/hco/5/GRCh38#64718822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104980932-A-C

64718857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980910-T-C

64718999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980811-G-T

64719002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980808-T-C

http://identifiers.org/hco/5/GRCh38#64719038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104980774-C-A

64719067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980758-T-C

http://identifiers.org/hco/5/GRCh38#64719070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104980755-C-A

64719070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980755-C-T

64719135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980693-T-C

64719233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980599-A-G

64719446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104980332-T-C

64719645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979948-T-C

64719697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979714-C-T

64719953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979500-G-T

http://identifiers.org/hco/5/GRCh38#64719979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104979474-C-A

64719985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979467-T-C

http://identifiers.org/hco/5/GRCh38#64720045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104979439-C-A

64720050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979434-G-A

64720225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979290-C-T

64720271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979244-T-C

64720291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104979223-T-C

http://identifiers.org/hco/5/GRCh38#64720964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104978902-C-A

64720964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104978902-C-T

http://identifiers.org/hco/5/GRCh38#64721085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104978786-C-A

64721097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104978774-T-C

http://identifiers.org/hco/5/GRCh38#64721243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104978647-C-A

64721469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104978506-T-C

64721545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104978429-T-A

64721603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104978380-G-A

64722272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104976816-G-A

64722272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104976816-G-T

64722648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975701-A-G

64722685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975667-T-C

64722717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975640-G-A

64722771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975580-A-G

64722978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975377-T-C

64723034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975321-A-G

64723256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975096-T-A

64723265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975087-T-G

64723331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104975022-A-G

64723590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974782-G-T

64723669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974704-G-A

64723669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974704-G-C

64723691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974683-A-G

64723727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974647-A-G

64723805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974572-C-T

64723929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974450-G-T

64723973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974414-A-G

http://identifiers.org/hco/5/GRCh38#64723977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104974410-C-A

http://identifiers.org/hco/5/GRCh38#64724034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104974366-C-A

64724085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974316-A-G

http://identifiers.org/hco/5/GRCh38#64724099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104974302-C-A

64724179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974234-C-G

64724299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974139-G-A

64724299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974139-G-T

http://identifiers.org/hco/5/GRCh38#64724313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104974124-A-C

http://identifiers.org/hco/5/GRCh38#64724329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104974109-C-A

64724329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974109-C-T

64724367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 3 prime UTR variant
orthologous variants: 104974071-T-C

http://identifiers.org/hco/5/GRCh38#64724408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104974030-A-C

64724870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104973621-T-A

64725194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104973065-G-T

64725274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104972986-A-G

64725301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104972961-C-T

64725391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104972877-C-T

64725417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104972854-G-T

64725512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104972111-T-C

64727140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104971541-T-C

64727890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104971226-T-C

64727895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104971221-C-T

64727926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104971188-A-T

64727956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104971161-T-A

64728036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104970905-A-G

64728038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104970903-A-G

64728048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104970894-A-G

http://identifiers.org/hco/5/GRCh38#64728065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104970877-C-A

64728065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104970877-C-G

64728101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104970832-A-G

64728104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104970829-T-C

64728249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104970686-A-G

http://identifiers.org/hco/5/GRCh38#64728258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104970677-A-C

64728258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104970677-A-G

64739971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104970341-C-G

64739971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104970341-C-T

64739997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104970321-T-A

64740007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104970313-T-C

64740053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104970269-T-A

64740664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969759-C-T

64740845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969700-C-G

64740884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969660-T-A

64740954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969594-C-T

64740968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969580-G-T

64740981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969573-G-C

64740981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969573-G-T

64741037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969523-T-C

64741047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104969513-T-C

64741049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104969511-T-C

http://identifiers.org/hco/5/GRCh38#64741167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104969393-A-C

64741167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104969393-A-T

http://identifiers.org/hco/5/GRCh38#64741218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104969342-A-C

http://identifiers.org/hco/5/GRCh38#64741279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104969289-C-A

64741279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969289-C-T

64741301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969273-T-C

64741301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969273-T-G

64741308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969266-T-C

64741308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969266-T-G

64741321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969256-G-T

64741330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969248-T-C

64741335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969243-T-C

http://identifiers.org/hco/5/GRCh38#64741336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104969242-C-A

64741336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969242-C-T

64741345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969233-G-T

64741352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969228-G-A

64741352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104969228-G-T

64741476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104968924-G-A

64741477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104968923-T-A

64741571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104968835-C-T

64741648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104968764-A-G

64741648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104968764-A-T

64741676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104968736-G-C

http://identifiers.org/hco/5/GRCh38#64741738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104968671-A-C

64744764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104968048-A-G

64744764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104968048-A-T

64744811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104968001-G-A

64744811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104968001-G-T

64744849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967974-G-A

64744955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967860-T-C

64745036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967779-T-A

64745121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967717-T-C

64745145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967693-C-T

64745218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967629-T-C

64745251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967599-T-G

64745606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967550-G-T

64745649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967510-T-C

64745753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967443-T-G

64745764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967438-G-A

64745819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967380-G-A

64745943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104967243-T-A

64754201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963718-G-A

64754201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963718-G-T

64754431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963497-G-A

64754431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963497-G-T

64754448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963488-A-G

64754458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963478-A-G

64754794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963464-A-T

64755758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963313-T-A

64755917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963231-T-C

64755960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104963184-A-G

64756237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962900-T-C

64756257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962879-T-C

64756429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962760-G-A

64756475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962726-T-G

64756529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962674-T-A

64756577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962635-T-C

64756605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962608-T-C

64758210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962040-C-G

64758210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104962040-C-T

64758437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104961807-T-C

64758543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104961688-A-T

http://identifiers.org/hco/5/GRCh38#64758683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104961561-A-C

64758742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104961498-C-T

64758757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104961481-C-T

64759179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104961007-C-G

64759216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104960977-G-A

64759216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104960977-G-C

64759447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104960753-T-C

http://identifiers.org/hco/5/GRCh38#64759643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104960540-A-C

64759643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104960540-A-G

64760001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104960203-A-G

64762470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104958511-G-T

64762568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104958413-A-G

64762665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104958321-T-G

64763743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104957707-T-C

64764478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104957421-C-T

64765122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104956805-C-G

64765551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104956412-G-A

64765551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104956412-G-T

64765559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104956404-G-A

64765733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104956224-A-G

64765733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104956224-A-T

64766042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104955947-G-A

http://identifiers.org/hco/5/GRCh38#64766244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104955758-A-C

64766368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104955643-T-C

64766450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104955569-T-C

http://identifiers.org/hco/5/GRCh38#64766867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104955187-C-A

64766867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104955187-C-T

http://identifiers.org/hco/5/GRCh38#64767048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104955127-A-C

http://identifiers.org/hco/5/GRCh38#64768039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104954325-C-A

64768041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104954323-G-A

64768098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104954275-T-C

64768144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104954232-A-G

64768174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104954202-G-A

64768456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 104953921-T-G

64768576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 104953800-C-G

http://identifiers.org/hco/5/GRCh38#64768580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#104953796-C-A

64768580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 104953796-C-T

http://identifiers.org/hco/5/GRCh38#64768594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#104953782-C-A

64768594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 104953782-C-T

http://identifiers.org/hco/5/GRCh38#64768648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#104953733-C-A

64768648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104953733-C-G

64768648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104953733-C-T

64768656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104953725-G-A

64768656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104953725-G-C

64768656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104953725-G-T

http://identifiers.org/hco/5/GRCh38#64768690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#104953690-A-C

64768690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26716
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104953690-A-G