150870541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58697104-C-G

http://identifiers.org/hco/3/GRCh38#150870918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58697437-A-C

http://identifiers.org/hco/3/GRCh38#150870964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58697473-A-C

150870964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58697473-A-G

150871005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58697507-T-G

150871007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58697509-C-T

150871117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58697613-T-C

150871547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58697930-T-A

150872478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698517-G-A

150872802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698746-T-C

150872816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698760-C-T

150873009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698964-C-G

http://identifiers.org/hco/3/GRCh38#150873112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58699053-C-A

150873167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699104-C-T

http://identifiers.org/hco/3/GRCh38#150873252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58699189-C-A

150873252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699189-C-T

150873478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699411-G-T

150873490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699423-G-A

150873490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699423-G-T

150873654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58699587-A-G

150874805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58702814-C-T

150875174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58703516-T-G

150875876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58704871-G-A

150875880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58704875-C-G

150875932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58704932-A-G

150876329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58705319-A-T

150876360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58705350-T-C

150876429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58705419-C-T

150876515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58705500-A-G

150876545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58705530-G-T

150876736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58705723-G-A

150877227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58706220-G-A

150877314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58706324-T-C

150877570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58706584-A-G

150877584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58706598-C-G

150877762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58706945-C-T

150877766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58706949-T-G

150877981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707146-G-A

150878085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707247-T-G

150878182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707324-A-G

150878223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707371-C-G

150878223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707371-C-T

150878258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707405-A-T

150878279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707428-C-T

150878435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58707614-A-G

150878879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58708069-T-C

150879336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58708496-T-C

150880957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58709779-C-T

150881935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58710272-G-A

150882021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58710376-C-T

150882342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58710618-C-T

150882387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58710663-C-T

150882406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58710672-T-A

150882622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58710814-G-A

150882770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711021-G-A

150882770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711021-G-C

150882787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711038-A-G

150882810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711092-G-A

150882810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711092-G-T

150882816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711098-G-T

http://identifiers.org/hco/3/GRCh38#150882826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58711103-A-C

150882826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711103-A-G

150883093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711369-G-A

150883093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711369-G-T

http://identifiers.org/hco/3/GRCh38#150883309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58711643-A-C

150883309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711643-A-G

150883346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711679-A-G

http://identifiers.org/hco/3/GRCh38#150883352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58711685-A-C

150883374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711707-C-T

150883464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711778-G-A

150883464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711778-G-C

150883497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711810-C-T

http://identifiers.org/hco/3/GRCh38#150883550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58711850-C-A

150883550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711850-C-T

http://identifiers.org/hco/3/GRCh38#150883551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58711851-C-A

150883551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711851-C-T

150883552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711852-G-A

150883552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58711852-G-T

http://identifiers.org/hco/3/GRCh38#150883910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58712107-C-A

150883914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58712111-C-T

150883984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58712181-G-A

150884173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58712374-G-A

http://identifiers.org/hco/3/GRCh38#150884332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58712484-C-A

150884332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58712484-C-G

150884351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58712503-A-G

150884415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58712556-A-T

150884660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713483-T-C

150884660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713483-T-G

150884757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713582-G-A

150884799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713625-C-G

150884822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713640-C-G

150885305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713921-G-A

150885332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713947-A-G

150885345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713960-G-C

150885353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713968-A-G

150885354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58713969-T-C

150885842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58714359-G-A

150885904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58714414-C-T

http://identifiers.org/hco/3/GRCh38#150885950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58714461-A-C

150885950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58714461-A-G

150886004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58714519-C-G

http://identifiers.org/hco/3/GRCh38#150886133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58714606-A-C

150886133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58714606-A-G

150886367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58714816-C-T

150886562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58715030-C-T

http://identifiers.org/hco/3/GRCh38#150888316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58715863-C-A

150888524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58716100-C-G

150888597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58716161-C-T

150889740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58716579-G-A

150889842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58716694-T-C

150889877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58716716-G-T

http://identifiers.org/hco/3/GRCh38#150890200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58717016-A-C

150890363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58717182-T-A

150890433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58717252-A-G

http://identifiers.org/hco/3/GRCh38#150890528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58717341-C-A

150890528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58717341-C-T

150890562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58717375-T-A

http://identifiers.org/hco/3/GRCh38#150890601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58717414-C-A

150890603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58717417-T-C

150890820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58717712-C-T

150890821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58717713-A-G

150890922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58717804-G-A

http://identifiers.org/hco/3/GRCh38#150890939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58717820-C-A

150890939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58717820-C-T

150890974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58717855-C-T

http://identifiers.org/hco/3/GRCh38#150891055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58717936-C-A

150891055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58717936-C-T

150891060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58717941-C-G

150891060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58717941-C-T

150891118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58717999-G-A

150891118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58717999-G-T

150893273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719218-T-C

150893445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719392-A-T

http://identifiers.org/hco/3/GRCh38#150893526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58719531-C-A

150893526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719531-C-T

150893653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719654-C-T

150893654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719655-A-G

150893654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719655-A-T

150893672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719671-C-T

150893695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719694-T-A

150893695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719694-T-C

150893695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719694-T-G

150893696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719695-T-G

150893707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719706-G-T

150893709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719708-G-C

150893709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719708-G-T

150893710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719709-G-A

150893710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719709-G-C

150893961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719876-G-A

150894027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719934-A-G

150894084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719979-G-C

150894084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58719979-G-T

http://identifiers.org/hco/3/GRCh38#150894175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58720045-C-A

150894180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58720050-T-C

150894291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58720161-G-T

150894356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58720240-A-G

150894434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58720302-C-G

150894641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58720532-C-G

150896800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58720967-T-C

150897001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721169-G-A

150897241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721354-G-C

150897331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721406-G-C

150897390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721436-A-G

150897549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721588-G-A

150897855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721856-C-T

150897857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721858-A-G

150897937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58721935-G-A

150897972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58722446-G-A

150898093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58722543-G-A

150898136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58722586-A-G

http://identifiers.org/hco/3/GRCh38#150898143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58722593-C-A

150898143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58722593-C-T

150898251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58722689-G-A

150898268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58722706-G-A

150898452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58722875-G-A

150899872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58724478-A-G

150900051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58724656-C-G

150901050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58725538-C-G

150901081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58725568-C-T

150901145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58725638-A-G

http://identifiers.org/hco/3/GRCh38#150901333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58726134-C-A

150901362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58726160-G-T

150902143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58726399-T-C

150902174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58726421-T-C

150902275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58726494-T-G

150902377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58726569-G-A

150902457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58726646-G-A

150902457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58726646-G-T

http://identifiers.org/hco/3/GRCh38#150902464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58726653-C-A

150902761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58726975-C-T

150902923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58727154-A-G

150903315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58727542-A-G

150903324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58727551-G-A

150903325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58727552-C-T

150903331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 58727558-G-T

150903335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58727562-G-A

150903352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58727579-T-A

150903352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58727579-T-C

150903365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58727592-G-C

http://identifiers.org/hco/3/GRCh38#150903392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58727619-C-A

150903392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58727619-C-T

http://identifiers.org/hco/3/GRCh38#150903453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58727675-C-A

150903528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58727730-A-G

150903553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58727754-G-T

150903770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58727966-A-G

150903900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58728080-T-A

http://identifiers.org/hco/3/GRCh38#150904227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58728440-C-A

150904345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58728566-T-G

150904406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58728628-G-A

http://identifiers.org/hco/3/GRCh38#150904483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58728702-C-A

150904756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58728966-G-T

http://identifiers.org/hco/3/GRCh38#150904965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58729164-C-A

150904970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729169-T-G

150905106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729334-A-G

150905148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729376-A-G

150905201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729430-A-G

150905353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58729646-T-C

150905375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58729668-C-T