http://identifiers.org/hco/1/GRCh38#35573373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629977-C-A

35573373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629977-C-T

35573376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629974-G-A

35573376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629974-G-T

http://identifiers.org/hco/1/GRCh38#35573397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629953-C-A

35573397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629953-C-T

35573422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629928-G-T

http://identifiers.org/hco/1/GRCh38#35573431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629919-C-A

35573431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629919-C-T

35573436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629914-T-A

35573436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629914-T-C

35573436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629914-T-G

35573445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629905-G-A

35573445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629905-G-C

35573445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629905-G-T

http://identifiers.org/hco/1/GRCh38#35573469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629881-A-C

35573496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629854-T-C

35573496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629854-T-G

35573534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629826-G-T

35573544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126629816-G-A

35573679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126629680-T-A

35573679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126629680-T-C

35573718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629633-G-T

http://identifiers.org/hco/1/GRCh38#35573728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629622-C-A

http://identifiers.org/hco/1/GRCh38#35573731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629619-C-A

35573746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629595-G-A

35573746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629595-G-C

35573746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629595-G-T

35573759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629584-G-A

35573800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629553-A-G

http://identifiers.org/hco/1/GRCh38#35573802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629551-A-C

35573883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629487-T-C

35573961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629409-G-A

35573961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629409-G-T

http://identifiers.org/hco/1/GRCh38#35574138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629232-C-A

35574138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629232-C-G

35574138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629232-C-T

35574140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629230-G-A

35574140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629230-G-T

35574170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 126629200-G-A

35574170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 126629200-G-C

35574170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 126629200-G-T

http://identifiers.org/hco/1/GRCh38#35574206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629164-C-A

35574206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629164-C-T

http://identifiers.org/hco/1/GRCh38#35574209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629161-C-A

35574209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629161-C-G

35574209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629161-C-T

http://identifiers.org/hco/1/GRCh38#35574216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126629154-C-A

35574216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629154-C-G

35574216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 126629154-C-T

35574472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126628901-A-G

35574497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126628875-G-A

35574497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126628875-G-T

35574617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126628777-G-A

35574617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126628777-G-T

35574687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126628685-G-T

35574700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126628673-T-C

35574712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628661-A-G

35574714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628659-G-A

35574714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628659-G-T

35574800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628583-T-A

35574843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628531-G-C

35574914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628477-T-C

35575025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628360-A-G

http://identifiers.org/hco/1/GRCh38#35575060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126628339-A-C

http://identifiers.org/hco/1/GRCh38#35575097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126628298-C-A

35575097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628298-C-T

35575119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628276-A-G

35575144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628255-A-G

35575144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628255-A-T

http://identifiers.org/hco/1/GRCh38#35575147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126628252-C-A

35575147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628252-C-T

35575155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628244-C-T

35575221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126628188-G-A

35575993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126627420-T-C

http://identifiers.org/hco/1/GRCh38#35576750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126626815-A-C

35576875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126626705-G-A

35577020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126626591-C-T

35577357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 126626435-G-T

35577490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126626304-G-A

35577490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126626304-G-T

35577511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126626280-G-T

http://identifiers.org/hco/1/GRCh38#35577548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126626238-C-A

35577642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126626157-A-G

35577662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126626136-G-T

35577670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126626128-T-C

35577730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126626067-A-G

http://identifiers.org/hco/1/GRCh38#35577829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126625979-C-A

35577829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126625979-C-T

35577870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126625937-A-G

35577949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126625858-C-T

35577992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126625808-A-G

35578491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126625479-G-A

35578664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126625325-C-T

35583601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126620797-G-A

35585013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126618796-T-C

35585149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126618668-A-T

35585654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126618317-T-C

35586413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126617184-G-A

35586749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126616944-G-A

35587058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126616678-G-C

35587149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126616588-C-G

35587245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126616501-G-A

35587300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126616451-G-T

35587901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126616257-G-A

35587902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126616256-G-A

http://identifiers.org/hco/1/GRCh38#35588268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126616014-C-A

http://identifiers.org/hco/1/GRCh38#35588270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126616012-C-A

35588270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126616012-C-G

35588270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126616012-C-T

35588289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615953-G-A

35588289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615953-G-T

http://identifiers.org/hco/1/GRCh38#35588295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126615947-C-A

35588295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615947-C-T

35588362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126615836-G-A

35588366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126615832-T-G

35588491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126615707-C-G

35588491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 126615707-C-T

http://identifiers.org/hco/1/GRCh38#35588530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126615668-C-A

35588565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615633-G-A

35588565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615633-G-T

http://identifiers.org/hco/1/GRCh38#35588603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126615588-C-A

35588649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615531-C-T

35588652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615528-T-C

35589108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615205-G-A

35589200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615124-G-C

35589223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615096-T-C

35589233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126615086-T-A

35589493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126614821-C-T

35589647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126614701-G-A

35589660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126614688-C-G

35589778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126614550-T-C

35589785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126614536-A-G

35589837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126614492-T-G

35589973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126614352-G-C

35590062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126614263-G-A

35590095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126614239-T-A

35590095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126614239-T-C

35590162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126614183-A-T

35590165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126614180-G-T

35590562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613410-G-A

35590562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613410-G-T

35590571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613401-T-C

35590571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613401-T-G

35590593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613379-A-G

35590595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613377-A-G

35590696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126613282-G-A

35590726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126613252-G-A

35590726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126613252-G-T

http://identifiers.org/hco/1/GRCh38#35590747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126613231-A-C

35590747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126613231-A-G

35590786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613192-G-A

35590786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613192-G-T

http://identifiers.org/hco/1/GRCh38#35590787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126613191-C-A

35590787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126613191-C-T

35591483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126612363-G-A

35591562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126612315-C-G

35593524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126611493-C-T

35594189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610932-T-C

35594207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610916-G-A

http://identifiers.org/hco/1/GRCh38#35594255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126610868-C-A

35594255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610868-C-T

http://identifiers.org/hco/1/GRCh38#35594264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126610859-C-A

35594278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610845-T-C

35594286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610837-G-T

35594294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610831-A-G

http://identifiers.org/hco/1/GRCh38#35594342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126610640-C-A

35594348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610634-G-A

35594348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610634-G-C

35594348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610634-G-T

http://identifiers.org/hco/1/GRCh38#35594349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126610633-C-A

35594359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126610623-T-C

35594460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126610520-A-G

35594518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126610462-C-T

35594612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126610368-G-A

35594617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126610363-G-A

35594620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126610360-G-A

35594621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126610359-G-A

35594623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126610357-A-G

35594765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610232-G-A

35594825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610177-G-A

35594825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610177-G-C

35594840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610164-G-T

35594841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610163-G-A

35594841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610163-G-C

35594841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610163-G-T

35594845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610159-G-A

35594845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610159-G-T

http://identifiers.org/hco/1/GRCh38#35594939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126610128-C-A

35594939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610128-C-T

35594941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610126-G-T

35594977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126610090-A-G

35595114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126609993-T-A

35595114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126609993-T-C

35595114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126609993-T-G

35595189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126609926-T-G

http://identifiers.org/hco/1/GRCh38#35595193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126609922-C-A

35595193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126609922-C-T

http://identifiers.org/hco/1/GRCh38#35595207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126609908-A-C

35595207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126609908-A-G

35595388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3 prime UTR variant
orthologous variants: 126609729-A-G

http://identifiers.org/hco/1/GRCh38#35595403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126609714-C-A

35595403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30774
most severe consequence: 3 prime UTR variant
orthologous variants: 126609714-C-T