http://identifiers.org/hco/4/GRCh38#107824625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#131196355-C-A

107824625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131196355-C-T

107824761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131196205-C-T

http://identifiers.org/hco/4/GRCh38#107824788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131196170-C-A

107824813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131196147-T-C

http://identifiers.org/hco/4/GRCh38#107824894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#131196102-C-A

107824894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 131196102-C-T

107824956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131196045-G-A

107824956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131196045-G-T

107825086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131195952-G-A

107825086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131195952-G-T

107825176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131195913-G-A

107825176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131195913-G-T

107825211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131195882-A-G

107825211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131195882-A-T

107825217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131195876-T-C

107825517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131195595-C-T

107825541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131195570-G-A

http://identifiers.org/hco/4/GRCh38#107825649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131195528-A-C

107825649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131195528-A-T

107825859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131195341-A-G

107826134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131195104-G-A

http://identifiers.org/hco/4/GRCh38#107826310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131194942-A-C

107826310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194942-A-T

107826426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194829-G-A

107826426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194829-G-T

107826560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194625-C-T

107826600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194585-G-C

107826644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194534-G-C

107826644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194534-G-T

107826752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131194428-C-T

107827112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131193978-A-T

107827365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131193613-T-A

107827484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131193508-A-G

107828433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131192769-A-G

107828857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131192081-G-A

107829284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131191490-G-A

107829363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131191272-T-G

107829462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131191175-A-G

107829520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131191117-A-G

107829638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131190999-G-A

107829638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131190999-G-T

107830879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131189341-A-G

107830956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131189249-A-G

107831188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131189045-C-G

107831276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131188962-C-G

107831276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131188962-C-T

107831466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131188560-C-T

107831498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131188528-C-T

107831776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131188318-T-C

107831820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131188278-A-G

107831929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131188173-T-C

107835638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131184834-A-G

107835659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131184464-A-G

107835770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131184349-G-T

107835909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131184019-A-G

107835962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183964-G-A

107835998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183934-C-G

107836101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183832-A-T

107836136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183795-A-T

107836182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183768-G-A

107836740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183183-G-A

107836740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183183-G-T

107836799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183085-G-T

107836832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131183056-G-C

107836950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182996-T-C

107837060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182863-C-G

107837075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182814-C-T

107837320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182460-T-C

107837345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182436-A-G

107837425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182357-T-C

107837483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182304-G-A

107837483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131182304-G-C

107837837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131181957-T-C

107837890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131181925-G-T

107838921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131180166-C-T

107839268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131179735-A-G

107839334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131179637-C-T

107839347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131179608-G-A

107839355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131179600-G-T

107839367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131179587-G-A

107839367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131179587-G-T

107841518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

107843199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131177161-A-G

107843279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131177079-T-A

107843384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131176983-A-G

107843507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131176840-C-T

107843559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131176792-G-C

107843665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131176678-A-G

107843694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131176646-G-C

107843913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131176487-G-T

107851103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131172065-C-G

107851788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131170826-G-A

107851914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131170701-C-T

http://identifiers.org/hco/4/GRCh38#107851985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131170619-C-A

107851985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131170619-C-T

107852053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131170556-A-G

107852062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131170547-G-A

107852161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131170483-T-C

107852789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131169870-C-T

107852812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131169849-T-C

107853118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131169564-T-C

107853187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131169503-A-T

107853423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131169250-T-A

107854290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166911-G-A

107854510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166741-T-G

107859438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166592-C-T

107859501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166531-G-A

107859616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166420-G-A

107859616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166420-G-T

107859643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166399-A-G

107859893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166170-T-C

http://identifiers.org/hco/4/GRCh38#107859944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131166112-A-C

107860054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131166041-C-T

http://identifiers.org/hco/4/GRCh38#107860056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131166039-A-C

107861120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131160554-G-A

107861152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131160524-T-G

107861491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131160209-G-A

107861711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131160045-A-G

107861712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131160044-A-G

107861737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131159835-T-C

107862184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131159332-G-A

107862274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131159170-C-G

107862274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131159170-C-T

107862305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131159140-A-G

107862639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158678-G-A

107862699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158620-G-A

107863156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158194-G-A

107863156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158194-G-T

107863159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158191-A-G

107863181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158169-C-T

107863185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158165-A-G

107863222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131158121-G-A

107863351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131157997-A-G

107863362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131157986-T-A

107863435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131157924-G-A

107863435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131157924-G-C

107863435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131157924-G-T

107863446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131157904-A-G

http://identifiers.org/hco/4/GRCh38#107863623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131157756-C-A

107863623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157756-C-G

107863623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157756-C-T

107863666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157732-C-G

107863698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157709-T-C

107863730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157677-T-C

107863730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157677-T-G

http://identifiers.org/hco/4/GRCh38#107863857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131157565-C-A

107863857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157565-C-T

107863881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157550-T-C

107863968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157473-G-T

107864075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157367-G-T

http://identifiers.org/hco/4/GRCh38#107864116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#131157335-C-A

107864223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 131157300-T-C

107864258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 131157266-G-A

107864324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 131157212-T-G

107864390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157158-T-C

107864391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131157157-C-T

107864559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131156994-T-C

http://identifiers.org/hco/4/GRCh38#107865614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131155777-C-A

107865653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131155735-C-G

107865653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131155735-C-T

107865697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131155694-A-G

107865833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131155083-A-T

http://identifiers.org/hco/4/GRCh38#107865871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131155043-C-A

107865940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131154961-A-G

http://identifiers.org/hco/4/GRCh38#107866066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131154852-A-C

107866224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131154708-T-C

107866908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 131154054-C-T

107866931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131154031-G-A

http://identifiers.org/hco/4/GRCh38#107866940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131154024-C-A

107866973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131153999-A-G

http://identifiers.org/hco/4/GRCh38#107867116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131153862-C-A

107867124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131153854-A-G

107867153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131153824-G-T

http://identifiers.org/hco/4/GRCh38#107867176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131153808-C-A

http://identifiers.org/hco/4/GRCh38#107867241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131153734-C-A

107867508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131153520-T-C

http://identifiers.org/hco/4/GRCh38#107868173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131152271-A-C

107868291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131152147-C-G

107869455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131151259-T-A

107869455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131151259-T-C

107869863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131150631-T-C

107869916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131150582-G-A

107869992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131150518-G-A

107870055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131150405-C-T

http://identifiers.org/hco/4/GRCh38#107870368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131149717-A-C

107870479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131149605-G-A

107870709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131149194-A-G

107870990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131148948-A-G

107874748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131147916-T-C

107875747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131147367-T-C

107875754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131147360-T-A

107875810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131147304-A-T

107876537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146961-G-A

107876593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146907-T-C

107876595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146905-T-G

107876610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146886-A-G

107876627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146869-A-G

107876669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146837-A-G

107876713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146799-G-A

107877329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146506-C-T

107877586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131146259-A-T

107878624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146103-A-T

107878680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131146046-C-T

http://identifiers.org/hco/4/GRCh38#107878860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131145464-A-C

107879069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131145274-T-C

107879074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131145269-T-A

107879278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144922-A-G

107879398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144769-G-A

107879442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144731-A-G

107879447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144726-T-A

107879485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144650-C-G

107879485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144650-C-T

107879496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144639-C-T

107879752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144530-G-A

107879934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144346-T-G

107880071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144221-T-C

107880153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131144138-C-T

107880457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131143469-G-C

107880973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131143316-A-G

http://identifiers.org/hco/4/GRCh38#107882575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131142623-C-A

107882645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131142561-A-G

107882660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131142546-A-G

107882882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131142335-A-G

107882882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131142335-A-T

107883214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131141984-G-A

107883214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131141984-G-C

107883214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131141984-G-T

107892915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138904-T-A

107893071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138751-T-C

107893152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138665-T-C

107893169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 131138644-A-G

107893469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138416-G-T

107893518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138369-G-A

107893533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138354-A-G

107893552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138335-C-G

107893552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138335-C-T

107893585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131138314-T-C

107893691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138220-T-C

http://identifiers.org/hco/4/GRCh38#107893708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131138203-C-A

107893708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138203-C-T

107893743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138161-A-G

107893780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138120-G-T

107893787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138113-T-C

107893807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138094-A-G

107893841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131138060-A-G

107893976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137532-C-T

107894115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137400-T-C

http://identifiers.org/hco/4/GRCh38#107894139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131137376-C-A

107894139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137376-C-T

107894167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137348-A-G

http://identifiers.org/hco/4/GRCh38#107894186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131137342-C-A

107894187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137341-T-A

107894187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137341-T-C

107894187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137341-T-G

107894225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137323-A-G

107894233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137315-G-A

107894233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131137315-G-T

107894263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131137285-G-A

107894355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131137196-G-A

107894355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131137196-G-T

http://identifiers.org/hco/4/GRCh38#107894791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131136767-C-A

107894791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131136767-C-T

http://identifiers.org/hco/4/GRCh38#107894962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131136446-A-C

107895052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131136362-G-A

107895117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131136297-A-T

http://identifiers.org/hco/4/GRCh38#107895303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131136114-C-A

107895303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 131136114-C-T

107895313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131136104-G-T

107895369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131136054-G-A

107895547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131135877-G-A

107895547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131135877-G-C

http://identifiers.org/hco/4/GRCh38#107895605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131135819-A-C

107895605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131135819-A-G

107895615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131135809-C-G

107895615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131135809-C-T

http://identifiers.org/hco/4/GRCh38#107895619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131135805-C-A

107895619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131135805-C-T

107895809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131135615-G-A

107895809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131135615-G-T

107895845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131135579-A-G

107895965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131135459-T-G

107896027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131135399-T-C

107896037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131135389-G-A

107896037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131135389-G-T

107896080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131135345-A-G

107896138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131135290-A-G

107896325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131135121-G-A

107896385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131134954-G-A

107896431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131134916-T-C

107896431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131134916-T-G

107896784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131134579-T-C

107896958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131134404-A-T

107897027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131134338-C-T

107897249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131134201-A-G

http://identifiers.org/hco/4/GRCh38#107897267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131134183-C-A

107897307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131134143-C-G

107897437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131134008-G-A

107897783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133466-T-A

107897783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133466-T-C

107897942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133214-C-T

107898023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133147-T-G

107898026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133144-T-C

107898094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133076-T-A

107898154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133018-G-A

107898154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133018-G-C

107898176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131133000-G-A

107898251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131132946-G-A

107898251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131132946-G-C

107898275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131132922-A-T

107898451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131132749-C-G

107899241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131130366-G-A

107899393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131130213-C-T

http://identifiers.org/hco/4/GRCh38#107899561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131129942-A-C

107899561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131129942-A-G

107899651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131129853-A-G

107899652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131129852-C-T

107899687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131129817-C-T

http://identifiers.org/hco/4/GRCh38#107899701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131129806-C-A

107899701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131129806-C-G

107900248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131129402-A-G

107900486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131129172-A-G

107900515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131129145-T-A

107900579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131129102-A-G

107900622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131129059-T-C

107900795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128885-C-T

http://identifiers.org/hco/4/GRCh38#107900861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131128819-A-C

107900907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128771-C-T

107901074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128594-G-T

107901234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128443-A-G

107901453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128222-G-A

107901492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128181-C-T

http://identifiers.org/hco/4/GRCh38#107901554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131128135-C-A

http://identifiers.org/hco/4/GRCh38#107901573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131128121-A-C

107901592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128102-C-G

107901671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131128015-C-T

107901879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131127813-G-A

107902309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124977-C-G

107902309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124977-C-T

107902417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124877-C-T

107902722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124604-T-G

107902774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124563-T-G

107902846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124513-T-C

107902855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124508-A-G

107903112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124235-T-A

107903147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124191-T-A

107903147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131124191-T-G

107903397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131123959-G-C

http://identifiers.org/hco/4/GRCh38#107903399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131123957-C-A

107903399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131123957-C-T

107903413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131123942-C-G

107903425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131123930-G-A

107903510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131123847-T-A

107903538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131123798-T-C

107905806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121647-C-T

107905862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121606-G-A

107906025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121458-C-T

107906188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121339-T-C

107906354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121193-A-G

107906363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121184-T-C

107906399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121149-A-G

107906460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131121085-T-G

107906792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120641-G-A

107907094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120371-C-G

107907094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120371-C-T

http://identifiers.org/hco/4/GRCh38#107907117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131120345-C-A

107907162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120299-A-G

107907216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120244-G-T

107907309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120137-T-A

107907314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120132-T-C

http://identifiers.org/hco/4/GRCh38#107907351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131120101-C-A

107907351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131120101-C-T

107907692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119661-A-G

http://identifiers.org/hco/4/GRCh38#107908014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131119318-A-C

107908160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119179-T-G

107908212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119137-G-A

107908212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119137-G-C

107908212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119137-G-T

http://identifiers.org/hco/4/GRCh38#107908213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131119136-A-C

107908213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119136-A-G

107908217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119132-T-A

107908217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131119132-T-G

107908352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118999-G-A

107908352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118999-G-C

107908352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118999-G-T

http://identifiers.org/hco/4/GRCh38#107908369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131118982-C-A

107908369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118982-C-T

107908382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118970-C-T

107908657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118660-A-G

107908775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118542-G-A

http://identifiers.org/hco/4/GRCh38#107908776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131118541-C-A

107908776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118541-C-T

http://identifiers.org/hco/4/GRCh38#107908783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131118531-C-A

107908783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118531-C-G

107908783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118531-C-T

107908794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131118518-T-C

http://identifiers.org/hco/4/GRCh38#107908842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131118437-C-A

107909667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131117845-T-C

http://identifiers.org/hco/4/GRCh38#107909670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131117842-C-A

107909741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131117782-C-G

107909931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131117331-A-G

107910150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131117137-C-T

http://identifiers.org/hco/4/GRCh38#107910302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131117001-A-C

107910527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131116780-G-A

107910601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131116708-T-A

107910776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131116538-A-T

107910832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131116497-T-C

http://identifiers.org/hco/4/GRCh38#107910861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131116469-A-C

107911117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131116163-C-T

http://identifiers.org/hco/4/GRCh38#107911124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131116156-C-A

107911124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131116156-C-T

107911213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131116069-A-G

107911284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115998-C-T

http://identifiers.org/hco/4/GRCh38#107911395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131115919-C-A

107911454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115869-T-G

107911717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115606-A-G

107911817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115520-A-G

107911817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115520-A-T

107911839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115499-C-T

107911868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115468-G-C

107911868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115468-G-T

107912189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115194-G-A

107912189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115194-G-T

107912246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131115139-A-G

107912434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131114953-T-C

107912753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131114683-G-A

107912875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131114582-A-T

http://identifiers.org/hco/4/GRCh38#107912877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#131114580-C-A

107912887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131114570-G-A

107912887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131114570-G-T

107912977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131114528-T-G

107913306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131114167-T-A

107913484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131113995-G-A

107913768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131113727-G-A

107914400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131112916-T-A

107914758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131112350-G-C

107914758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28395
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131112350-G-T