http://identifiers.org/hco/6/GRCh38#170290760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#15596078-C-A

170290760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 15596078-C-T

170291156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15596463-G-A

170291156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15596463-G-C

http://identifiers.org/hco/6/GRCh38#170291158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15596465-C-A

170291158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15596465-C-G

170291158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15596465-C-T

http://identifiers.org/hco/6/GRCh38#170291217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15596524-C-A

170291217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15596524-C-T

http://identifiers.org/hco/6/GRCh38#170291257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15596565-C-A

170291399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15596714-G-C

170291402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15596717-C-T

170292315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15597613-C-T

170292486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15597807-C-T

170292880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15598185-A-G

170293184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15598518-G-A

170293506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15598824-G-A

170294312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15599562-G-A

170294653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15599877-C-G

170294653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15599877-C-T

170294966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15600173-C-G

170295006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15600234-A-G

170295881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, undefined
orthologous variants: 15600929-G-C

170295881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, undefined
orthologous variants: 15600929-G-T

http://identifiers.org/hco/6/GRCh38#170297094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15601671-C-A

170297228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, undefined
orthologous variants: 15601762-C-G

170297434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15601973-G-A

http://identifiers.org/hco/6/GRCh38#170297824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15602362-A-C

170297824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15602362-A-G

170298222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15602759-T-C

170298245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15602782-G-T

170298474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15602965-G-A

http://identifiers.org/hco/6/GRCh38#170298489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15602981-C-A

170298753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15603175-T-C

170298869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15603259-G-C

170298999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15603368-G-C

170299114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15603521-T-C

170299201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15603591-G-A

170299391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15603856-C-T

170299537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15604084-C-G

170299544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15604091-G-C

170299679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15604187-G-A

170299784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15604291-G-T

170303024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15604650-G-A

170303149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15604773-C-G

170304586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15606949-C-T

170304591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15606954-C-T

170304610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15606986-G-A

170304691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607055-G-T

170304795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607182-G-A

http://identifiers.org/hco/6/GRCh38#170304876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15607252-C-A

170304876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607252-C-G

170305270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607585-G-A

170305324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607637-G-A

170305447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607755-G-C

170305586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607870-C-T

170305595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607879-T-A

170305595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607879-T-C

170305608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15607882-G-A

170308011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15616948-C-T

170308065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15616984-C-G

170308086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15617005-A-G

170308209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15617081-C-T

170308564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15617391-T-C

170308633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15617451-G-A

170308717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15617478-C-T

170308723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15617484-A-G

170314456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15617940-A-G

170314657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15618170-C-G

170314691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15618200-T-A

http://identifiers.org/hco/6/GRCh38#170315339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15619410-C-A

170315450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15619515-G-T

170315452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15619517-C-T

http://identifiers.org/hco/6/GRCh38#170315500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15619575-A-C

170315500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15619575-A-G

170316226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15620038-C-G

170316274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15620099-T-G

170316485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15620286-A-G

170316523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15620352-G-T

http://identifiers.org/hco/6/GRCh38#170316574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15620403-C-A

170316644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15620450-T-A

170316744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15620546-A-G

170317064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15621729-C-T

170317098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15621761-T-A

170317141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15621800-C-G

http://identifiers.org/hco/6/GRCh38#170317251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15621893-C-A

170317251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15621893-C-T

170317261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15621903-A-G

http://identifiers.org/hco/6/GRCh38#170317292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15621924-C-A

170317292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15621924-C-G

170317388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15622021-G-C

170317396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15622029-T-C

170317414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15622047-A-G

170317414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15622047-A-T

170317429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15622062-C-G

170317429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15622062-C-T

170317513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15622146-T-C

170317561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15622194-T-G

170317634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15622267-G-A

170318349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15622982-G-A

170318461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15623052-A-G

170318569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15623052-A-G

170318890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15623052-A-G

170321818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625061-T-C

170322175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625391-T-A

170322191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625406-C-T

170322202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625416-C-T

170322424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625562-G-T

170322946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625885-T-C

170322999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625930-G-A

170322999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625930-G-T

170323012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625943-T-C

http://identifiers.org/hco/6/GRCh38#170323017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15625948-C-A

170323017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15625948-C-T

170323097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15626035-G-A

170330495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15627905-T-A

170330522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15627932-C-T

170330544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15627954-A-G

170330625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15628018-T-C

170330630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15628023-A-G

170330636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15628029-T-C

170346479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15633500-T-C

170346646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15633679-C-G

170347144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634063-A-G

170347156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634072-G-T

170347203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634117-T-C

170347410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634253-G-T

170347423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634263-T-A

170347680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634478-C-T

170347785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634581-G-A

170347968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634778-T-A

170348049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634863-G-T

170348054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634868-G-A

170348054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634868-G-T

170348064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15634878-G-T

170348224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 15635014-C-G

170348340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15635131-C-T

170348390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15635190-A-G

170348401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15635201-G-C

170348401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15635201-G-T

http://identifiers.org/hco/6/GRCh38#170348411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15635210-C-A

170348411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15635210-C-T

170348453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15635238-G-A

170348453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15635238-G-T

170358057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15637754-C-T

http://identifiers.org/hco/6/GRCh38#170358060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15637757-C-A

170358060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15637757-C-G

http://identifiers.org/hco/6/GRCh38#170358088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15637785-C-A

170358201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15637870-A-G

http://identifiers.org/hco/6/GRCh38#170358207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15637876-C-A

170358207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15637876-C-T

170358333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15637998-A-G

170358333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15637998-A-T

170358354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15638019-A-G

170358364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15638029-G-T

http://identifiers.org/hco/6/GRCh38#170387356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15641770-A-C

170387397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15641824-G-A

170387990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15642864-G-T

http://identifiers.org/hco/6/GRCh38#170387992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15642866-C-A

170388131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15643012-T-G

http://identifiers.org/hco/6/GRCh38#170388141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15643022-C-A

170388176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15643036-G-A

http://identifiers.org/hco/6/GRCh38#170388193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15643052-C-A

170388193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15643052-C-T

170388199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15643059-G-A

170388252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15643107-T-C

170388382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 15643235-C-G

170390002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15643708-G-A

170390555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15644198-C-T

http://identifiers.org/hco/6/GRCh38#170390890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15644427-C-A

170390890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15644427-C-T

170390902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15644435-G-A

170390902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15644435-G-T

170390905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15644438-T-C

170390906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15644439-T-G

170391081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 15644600-A-G

http://identifiers.org/hco/6/GRCh38#170391101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15644620-A-C

170391567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15644756-T-C

170395400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15646361-G-A

170395591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15646557-A-G

170395622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15646580-A-T

170395633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15646594-C-T

http://identifiers.org/hco/6/GRCh38#170395640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15646601-C-A

http://identifiers.org/hco/6/GRCh38#170395699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15646650-C-A

170395699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15646650-C-T

http://identifiers.org/hco/6/GRCh38#170395712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15646663-C-A

170395809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15646756-A-G

170402473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15649874-C-T

170402498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15649916-A-G

170402687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650007-G-A

170402687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650007-G-C

170402707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650024-C-G

170402911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650181-C-T

170402961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650240-G-A

170403199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650449-C-T

170403500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650742-G-A

170403692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: 15650956-A-T

http://identifiers.org/hco/6/GRCh38#170404130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15651401-C-A

170404188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15651476-G-A

170404188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15651476-G-T

http://identifiers.org/hco/6/GRCh38#170404198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15651486-C-A

170404198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15651486-C-T

http://identifiers.org/hco/6/GRCh38#170404457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15651747-A-C

170404457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15651747-A-G

http://identifiers.org/hco/6/GRCh38#170404466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15651756-C-A

170404493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15651785-T-C

170404566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15651855-G-A

http://identifiers.org/hco/6/GRCh38#170404609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15651898-C-A

170404609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 15651898-C-T

170404643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15651929-G-A

170404643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15651929-G-T

170404647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15651933-G-A

170404826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15652070-T-A

170404826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15652070-T-C

http://identifiers.org/hco/6/GRCh38#170404887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15652119-C-A

170404887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15652119-C-G

170404887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15652119-C-T

170404917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15652147-A-G

170404940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15652169-G-A

170404940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15652169-G-T

170405705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 15652796-C-G

170406330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653212-G-A

170406330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653212-G-T

170406389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653271-G-A

170406389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653271-G-C

170406389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653271-G-T

170406411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653283-G-A

http://identifiers.org/hco/6/GRCh38#170406486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#15653362-C-A

170406905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653706-T-C

170407047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653829-A-G

170407052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21109
most severe consequence: 3 prime UTR variant
orthologous variants: 15653834-T-C