95517114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93694795-A-T

95517174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93694743-G-T

95517597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93694345-T-G

http://identifiers.org/hco/12/GRCh38#95517657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93694288-A-C

95517671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93694286-G-A

95517671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93694286-G-T

95517703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93694259-A-G

95518221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93693721-T-A

95520906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93692271-T-C

http://identifiers.org/hco/12/GRCh38#95520932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93692245-C-A

95520932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93692245-C-T

http://identifiers.org/hco/12/GRCh38#95520949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93692227-C-A

95520949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93692227-C-T

95520990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93692186-T-C

95520992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93692184-T-C

95521282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691894-T-A

95521282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691894-T-G

http://identifiers.org/hco/12/GRCh38#95521326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93691849-A-C

95521407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691756-A-G

95521483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691704-G-A

95521486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691701-A-T

http://identifiers.org/hco/12/GRCh38#95521568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93691632-C-A

95521611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691608-C-T

http://identifiers.org/hco/12/GRCh38#95521897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93691396-C-A

95521897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691396-C-T

95522052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93691282-T-C

95522202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691141-T-C

95522227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691116-C-T

95522259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93691080-G-T

95524545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93688799-T-C

95524620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93688762-A-T

95525781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93687328-G-C

95525815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93687312-G-A

95526007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93687191-C-T

95526170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93687049-T-C

http://identifiers.org/hco/12/GRCh38#95528658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93686374-C-A

95528687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93686343-T-C

http://identifiers.org/hco/12/GRCh38#95528732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93686273-C-A

http://identifiers.org/hco/12/GRCh38#95528739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93686266-C-A

95528739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93686266-C-G

95528977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93686035-T-A

95529023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685989-T-A

95529077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685941-T-A

95529077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685941-T-C

http://identifiers.org/hco/12/GRCh38#95529079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93685939-C-A

95529079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685939-C-T

95529090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685928-A-G

95529101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685914-G-A

95529101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685914-G-T

95529184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93685834-T-C

http://identifiers.org/hco/12/GRCh38#95532081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93683831-C-A

95532610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93683176-C-T

95532721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93683081-T-C

95532721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93683081-T-G

95532776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93683027-G-T

95532781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93683022-A-G

http://identifiers.org/hco/12/GRCh38#95532823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93682980-C-A

95532823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93682980-C-T

95532989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682814-T-C

http://identifiers.org/hco/12/GRCh38#95533004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93682799-C-A

95533168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93682635-A-G

95533178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682625-G-A

95533178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682625-G-C

95533263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682540-A-G

95533527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682273-T-C

95533548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682252-G-A

95533584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682216-T-C

95533702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93682092-T-A

95533706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682088-A-G

95533775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682022-A-G

95533788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93682009-G-A

95533788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93682009-G-T

95533818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93681979-A-G

95533883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93681914-G-A

http://identifiers.org/hco/12/GRCh38#95533894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93681903-C-A

95534006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93681791-T-C

95534086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93681711-T-C

http://identifiers.org/hco/12/GRCh38#95534227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93681570-A-C

95534227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93681570-A-G

95534383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93681410-T-C

http://identifiers.org/hco/12/GRCh38#95534384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93681409-C-A

95534384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93681409-C-T

95534466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93681324-C-T

95536898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679924-G-A

95536983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679851-G-A

95536987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679847-C-T

95537116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93679757-T-C

95538680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

95538707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

95538781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

95538955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

95539038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

95539091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

95539163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

95544479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93675478-T-G

95544660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93675344-T-G

95544671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93675333-G-A

95545121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93675015-A-G

95545212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674925-A-G

95545480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93674021-C-T

95545509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673991-A-G

95545530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673965-A-G

95545700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673802-A-G

95545790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673722-A-G

95545791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673721-T-C

95545807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673705-C-G

95545843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673669-C-T

95545879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673635-T-C

95546074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673450-A-T

95546213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673329-A-G

95546266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673279-T-G

95546298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673246-G-A

95546298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93673246-G-C

95546468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93673083-T-G

http://identifiers.org/hco/12/GRCh38#95546523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93673032-C-A

95546523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93673032-C-G

95546553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93673009-G-T

95546554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93673008-G-A

http://identifiers.org/hco/12/GRCh38#95546555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93673007-C-A

95546555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93673007-C-T

95546570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672992-C-G

95546593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672972-C-T

95546679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93672887-G-C

95546679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93672887-G-T

95546799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672778-T-C

95546799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672778-T-G

95546909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672605-G-A

95546926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93672580-G-T

95547208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93671387-A-G

95547319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93671257-C-T

95547334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93671188-A-G

95547676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670646-C-G

95547747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670565-C-T

http://identifiers.org/hco/12/GRCh38#95547751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670562-C-A

95547751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670562-C-T

95547907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670439-A-G

95547990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670370-T-C

95548032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93670331-C-T

http://identifiers.org/hco/12/GRCh38#95548059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670316-C-A

95548059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670316-C-T

http://identifiers.org/hco/12/GRCh38#95548063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670312-C-A

95548063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670312-C-T

95548126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670253-T-C

95548153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670237-G-A

95548153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670237-G-T

95548168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670227-G-A

95548168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670227-G-T

95548187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670214-G-A

95548187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670214-G-T

95548188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670213-C-T

95548219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670197-C-G

95548282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670144-G-A

95548287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670139-G-A

95548287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670139-G-T

http://identifiers.org/hco/12/GRCh38#95548299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670123-C-A

95548299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670123-C-T

http://identifiers.org/hco/12/GRCh38#95548327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670100-C-A

95548327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670100-C-T

http://identifiers.org/hco/12/GRCh38#95548343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670084-C-A

95548343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670084-C-G

95548343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93670084-C-T

http://identifiers.org/hco/12/GRCh38#95548348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670079-C-A

95548410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670072-T-C

http://identifiers.org/hco/12/GRCh38#95548415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670067-C-A

95548415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670067-C-T

95548443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670062-T-A

95548443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670062-T-C

http://identifiers.org/hco/12/GRCh38#95548444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93670061-C-A

95548444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670061-C-G

95548444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93670061-C-T

95548533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669980-T-C

95548560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669952-G-A

95548560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669952-G-T

http://identifiers.org/hco/12/GRCh38#95548640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93669878-C-A

95548640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669878-C-T

95548650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669868-T-C

http://identifiers.org/hco/12/GRCh38#95548711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93669810-C-A

95548711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669810-C-T

95548733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669787-G-A

95548733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93669787-G-T

http://identifiers.org/hco/12/GRCh38#95548763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93669759-A-C

95548763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93669759-A-G

95548808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669713-G-A

95548808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669713-G-C

95548808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669713-G-T

http://identifiers.org/hco/12/GRCh38#95548820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93669701-C-A

http://identifiers.org/hco/12/GRCh38#95548822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93669699-C-A

95548822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669699-C-G

95548822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669699-C-T

http://identifiers.org/hco/12/GRCh38#95548830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93669691-C-A

95548830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93669691-C-T

95548938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669598-T-C

95548958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669574-G-A

95548958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669574-G-C

95548958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669574-G-T

95548971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669561-G-A

95548971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669561-G-T

http://identifiers.org/hco/12/GRCh38#95548992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93669542-C-A

95548992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669542-C-G

95548992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669542-C-T

95549014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93669514-C-T

95550859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667822-T-G

95551037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93667698-C-G

95551273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 93667498-T-A

95551273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 93667498-T-C

95551282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93667489-C-G

95551293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93667478-T-A

95551361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93667382-G-A

95551389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93667351-T-A

95551389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93667351-T-G

95551434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93667316-A-G

95551446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93667304-G-T

http://identifiers.org/hco/12/GRCh38#95551492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93667258-C-A

http://identifiers.org/hco/12/GRCh38#95551544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93667199-C-A

95551544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 93667199-C-T

95551570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5 prime UTR variant
orthologous variants: 93667173-G-T

http://identifiers.org/hco/12/GRCh38#95551573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93667170-C-A

95551573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5 prime UTR variant
orthologous variants: 93667170-C-T

http://identifiers.org/hco/12/GRCh38#95551574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93667169-C-A

95551574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20064
most severe consequence: 5 prime UTR variant
orthologous variants: 93667169-C-T