150865456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58692054-T-A

http://identifiers.org/hco/3/GRCh38#150865800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58692583-A-C

150865800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58692583-A-G

150866648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58693142-G-A

http://identifiers.org/hco/3/GRCh38#150866676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58693170-C-A

http://identifiers.org/hco/3/GRCh38#150869254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58695766-A-C

150869341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58695858-G-C

150869560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696098-A-G

150869673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696226-C-T

150869907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696437-A-G

http://identifiers.org/hco/3/GRCh38#150869954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58696497-A-C

150870136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696681-G-A

150870157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696706-C-T

150870194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696740-T-G

150870541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697473-A-G

150871005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697507-T-G

150871007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697509-C-T

150871117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697613-T-C

150871547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58699189-C-T

150873478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58717182-T-A

150890433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 58717820-C-T

150890974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58717936-C-T

150891060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58717941-C-G

150891060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58717941-C-T

150891118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58720161-G-T

150894356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58727542-A-G

150903324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58727551-G-A

150903325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58727552-C-T

150903331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58727558-G-T

150903335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58727562-G-A

150903352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58727579-T-A

150903352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58727579-T-C

150903365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
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: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
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: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58729646-T-C

150905375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58729668-C-T

150905482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729775-G-T

150905568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729833-A-G

150905573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729838-G-A

150905573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729838-G-T

150905600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729865-G-A

150905600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729865-G-T

150905646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729889-G-A

150905646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58729889-G-C

150905756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730002-G-A

150905912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730136-G-A

150906060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730254-G-T

150906130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730328-T-A

150906131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730329-G-C

150906831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730609-A-G

150907012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730780-G-A

150907012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730780-G-T

150907203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730980-G-A

150907203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58730980-G-T

150907297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731063-G-T

150907567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731275-C-G

150907567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731275-C-T

150907571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731279-G-C

150907573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731281-G-A

150907706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731416-G-C

150907788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731467-A-G

150907808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731487-T-A

150907984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731594-T-C

150908053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58731656-A-G

150908216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733257-C-G

150908576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733440-G-A

150908651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733516-T-G

150908706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733573-G-A

150908749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733624-T-C

150908828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733695-G-A

150908844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733711-C-T

150908892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733758-C-T

150909031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58733883-C-G

150909307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58734136-C-T

http://identifiers.org/hco/3/GRCh38#150909358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58734187-A-C

150909404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58734218-G-A

150909530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58734372-G-T

150909539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58734381-G-A

150909713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58734534-G-A

150909745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58734568-G-A

150909769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58734582-C-T

http://identifiers.org/hco/3/GRCh38#150913064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58736207-A-C

150913066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58736209-A-G

http://identifiers.org/hco/3/GRCh38#150913351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58736434-C-A

150913385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58736458-A-G

150913497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58736568-G-A

http://identifiers.org/hco/3/GRCh38#150913530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58736601-A-C

150913566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58736633-G-C

150913569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58736636-T-G

150913855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58736902-G-C

150913901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737089-C-T

150913902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737090-A-T

150914041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737254-T-C

150914100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737313-G-A

150914183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737394-T-C

150914183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737394-T-G

150914212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737423-C-T

150914214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737425-C-G

150914237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737451-G-C

150914239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737453-C-T

150914303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737516-A-G

150914335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737548-T-C

150914421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737625-G-A

150914592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737793-T-C

150914773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58737958-C-T

150916035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738204-T-G

150916080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738245-C-G

150916087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738251-G-A

150916283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738447-C-T

http://identifiers.org/hco/3/GRCh38#150916295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58738459-C-A

150916295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738459-C-T

150916413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738539-C-G

150916427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738553-C-G

150916427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738553-C-T

150916431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738557-A-G

150916466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738590-C-T

150916597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738727-C-T

150916750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58738888-T-C

150917018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58739486-C-G

150917045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58739513-A-G

150917161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58739779-A-G

150917512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58740123-C-T

150917573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58740178-T-C

150917607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58740198-C-T

150918154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58740544-T-A

150918188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58740577-G-A

http://identifiers.org/hco/3/GRCh38#150918531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58740895-C-A

150918531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58740895-C-T

150918804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741137-G-T

150918903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741236-G-A

150918911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741244-C-T

150919076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741394-C-T

150919188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741503-C-T

150919274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741590-C-T

http://identifiers.org/hco/3/GRCh38#150919292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58741608-C-A

150919292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741608-C-T

150919304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741621-G-A

150919398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58741689-G-C

150919628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58749789-G-A

150919973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58750119-A-G

150920224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58750342-T-G

150920281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58750396-T-C

150926016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58751180-G-T

150926049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58751204-G-T

150926070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58751231-G-A

150926137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58751331-T-C

150926203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58751402-A-G

http://identifiers.org/hco/3/GRCh38#150926464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58751642-C-A

150926464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58751642-C-T

http://identifiers.org/hco/3/GRCh38#150926503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58751681-C-A

150926503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58751681-C-T

http://identifiers.org/hco/3/GRCh38#150926508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58751686-C-A

150926508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58751686-C-G

150926508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58751686-C-T

http://identifiers.org/hco/3/GRCh38#150926523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58751701-C-A

150926523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58751701-C-T

150926722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752048-A-G

150926783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752182-T-A

150926783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752182-T-C

150926851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752276-C-T

150926898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752323-C-T

150926927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752349-T-C

150927224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752686-G-T

150927255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752713-T-C

150927258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752716-G-A

150927273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58752783-A-G

http://identifiers.org/hco/3/GRCh38#150927522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58753172-C-A

150927522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753172-C-T

150927530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753180-T-A

150927530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753180-T-C

150927530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753180-T-G

150927531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753181-G-A

150927531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753181-G-T

http://identifiers.org/hco/3/GRCh38#150927662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58753336-A-C

150927662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753336-A-G

http://identifiers.org/hco/3/GRCh38#150927874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58753543-C-A

150928025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58753696-G-A

150928240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58753919-C-G

150928297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58753975-T-C

150928297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58753975-T-G

http://identifiers.org/hco/3/GRCh38#150928298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58753976-C-A

150928298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58753976-C-T

http://identifiers.org/hco/3/GRCh38#150928352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58754032-C-A

150928404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58754077-G-A

150928791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58754421-A-G

150928978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58754609-T-C

150929018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58754897-T-G

150929202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58755062-G-C

150929209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58755069-T-C

http://identifiers.org/hco/3/GRCh38#150929262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58755123-A-C

150929263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58755124-A-G

150929538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58755411-T-G

http://identifiers.org/hco/3/GRCh38#150929718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58755637-C-A

150929896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58755873-T-G

150929899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58755876-A-G

150930855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58756961-G-A

150931201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58757274-C-T

150931207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58757280-A-G

150931260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58757336-T-C

150931320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58757394-C-T

http://identifiers.org/hco/3/GRCh38#150931683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58757779-A-C

150931754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58757978-G-A

150931914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758137-C-G

150931914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758137-C-T

150932103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758303-A-G

150932129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758329-C-T

150932389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758584-C-G

150932389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758584-C-T

150932687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758849-G-A

150932837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58758988-C-T

150932976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58759127-C-G

150932976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58759127-C-T

150933063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58759189-T-C

150933124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58759222-A-G

150933135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58759233-T-A

150933136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58759234-G-C

150933617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58766926-G-A

150933869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58767127-C-T

150933927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58767166-C-T

150934150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58767351-T-C

http://identifiers.org/hco/3/GRCh38#150934228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58767415-A-C

150934245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58767437-G-T

150934330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58767525-A-G

150934508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58767604-G-A

150934775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58767735-T-C

150936292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58768065-A-G

150936354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58768126-G-A

150937229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58768758-A-G

150937487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58769004-T-A

150937544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58769062-T-C

150937945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58769408-C-T

150938351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58769865-T-C

150938351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58769865-T-G

150938613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58770120-T-C

150938769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58770265-C-T

150939043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58770503-G-C

150939910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58770769-C-T

http://identifiers.org/hco/3/GRCh38#150940356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58771289-C-A

150940356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58771289-C-T

150940363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58771296-G-A

150940363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58771296-G-T

150940578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58771504-G-T

150940818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58771709-G-A

150941082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58771957-C-T

150941154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772003-A-G

150941325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772163-T-A

http://identifiers.org/hco/3/GRCh38#150941374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58772207-C-A

150941374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772207-C-T

150941391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772224-G-A

150941391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772224-G-T

150941405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772238-T-C

150941466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772288-T-C

150941523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772336-C-T

150941565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772376-T-C

http://identifiers.org/hco/3/GRCh38#150941842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58772641-C-A

150941842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772641-C-G

150941881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772684-A-T

150941903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772713-A-T

150942009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58772815-T-C

http://identifiers.org/hco/3/GRCh38#150942473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58773299-C-A

150942473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58773299-C-T

150942479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58773305-T-C

150942479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58773305-T-G

http://identifiers.org/hco/3/GRCh38#150942659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58773476-C-A

http://identifiers.org/hco/3/GRCh38#150942731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58773536-C-A

150942731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58773536-C-T

150946417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58774942-G-A

150946447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58774984-T-A

150946502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58775035-A-T

150946555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58775100-T-G

150946586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58775119-G-A

150946638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58775171-A-G

150952847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58776006-T-C

150952847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58776006-T-G

http://identifiers.org/hco/3/GRCh38#150953091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58777447-A-C

150953125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58777405-C-T

150953264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58777279-A-G

150957585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58779218-C-T

150957607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58779232-C-T

http://identifiers.org/hco/3/GRCh38#150957953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58779491-A-C

150958094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58779602-G-A

150958380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58779874-C-T

150958557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58780018-A-G

150960314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58780850-G-A

150960383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58780931-G-A

150960507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781065-G-C

150960507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781065-G-T

150960641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781208-T-C

150960683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781251-G-A

150960755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781322-A-G

150960791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781359-T-C

150960998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781552-A-G

150961176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58781692-C-T

150961532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58782052-C-T

150961597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58782117-G-A

150961737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58782263-C-T

150961775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58782301-T-C

150961927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58782447-C-T

150962190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58782701-T-C

150962252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58782763-C-T

150962642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58784598-G-A

150962883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58784927-T-G

150962884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58784928-T-G

150962893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58784937-G-A

150965738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58786410-C-T

150966644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58786935-A-G

150966676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58786969-T-C

150967140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58787376-T-C

150967186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58787403-G-A

http://identifiers.org/hco/3/GRCh38#150967419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58787597-A-C

150967430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58787608-C-T

150967431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58787609-T-C

150967494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58787669-C-T

150967623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58787793-G-T

http://identifiers.org/hco/3/GRCh38#150967816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58787957-C-A

150968185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788334-T-C

150968192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788341-T-C

150968207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788356-A-G

150968256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788421-G-A

150968284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788485-G-A

150968294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788498-T-C

150968448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788633-A-G

150968702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58788890-T-C

150970130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58789623-T-C

150970510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58789996-T-C

150970823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58790336-C-T

150970847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58790358-A-G

150970865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58790375-C-T

150971676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58791211-G-A

150971686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58791221-T-C

150971686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58791221-T-G

http://identifiers.org/hco/3/GRCh38#150971949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58791475-C-A

150972147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58791647-A-T

150972239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58791992-G-A

http://identifiers.org/hco/3/GRCh38#150972276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58792029-A-C

150972371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792127-G-A

150972371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792127-G-C

150972371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792127-G-T

150972734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792487-G-A

http://identifiers.org/hco/3/GRCh38#150972740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58792493-C-A

150972754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792507-T-G

150972804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792557-C-T

150972993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792729-A-G

150972993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58792729-A-T

http://identifiers.org/hco/3/GRCh38#150973008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58792744-C-A

http://identifiers.org/hco/3/GRCh38#150973023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58792759-C-A

150973023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58792759-C-G

150973023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58792759-C-T

150973070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58792806-T-A

150973128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58792851-G-T

150973131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58792854-G-T

150973148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58792871-T-A

150973157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58792880-T-C

150973208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58792927-G-T

150973209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58792928-T-G

150973337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58793040-C-T

150973392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58793092-G-C

150973733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58793414-C-T

150973771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58793452-A-T

150974185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794131-T-C

150974342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794252-G-A

150974381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794291-T-G

150974385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794295-G-C

150974495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794396-A-G

150974556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794458-C-G

150974689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794579-A-G

150974880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794745-T-C

http://identifiers.org/hco/3/GRCh38#150975118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58794937-C-A

150975132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58794947-T-C

150975184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58795001-G-A

150975196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58795013-G-A

150975638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58795400-G-T

150976162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58795928-G-A

http://identifiers.org/hco/3/GRCh38#150976419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58796181-A-C

150976466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796225-C-T

150976474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796233-C-G

http://identifiers.org/hco/3/GRCh38#150976487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58796244-C-A

150976502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796260-A-G

150976587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796329-A-G

150976595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796337-A-T

150976650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796417-T-A

150976650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796417-T-C

150976785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58796524-A-G

http://identifiers.org/hco/3/GRCh38#150976999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58796670-C-A

150977453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58797092-C-T

150978176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58797644-C-T

http://identifiers.org/hco/3/GRCh38#150990298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58801297-C-A

150990298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58801297-C-T

http://identifiers.org/hco/3/GRCh38#150990374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58801371-A-C

150990425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58801420-T-C

150990436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58801431-T-G

150990553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58801546-A-T

150990803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58801802-G-T

150990845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58801863-C-G

150990873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58801891-A-G

150991044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58802061-G-C

150991282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58802193-A-G

150991447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58802380-G-A

150992216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58802980-A-G

150992432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58803162-C-T

150995078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58803937-G-A

150995398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804259-T-C

150995415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804266-C-G

150995415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804266-C-T

150995553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804460-G-A

http://identifiers.org/hco/3/GRCh38#150995586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58804491-A-C

150995634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804539-G-A

150995657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804551-G-A

150995672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804568-G-A

150995693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804589-G-A

150995704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804600-A-G

150995798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804686-G-A

150996005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58804885-T-C

150996293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805223-C-T

http://identifiers.org/hco/3/GRCh38#150996336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58805264-C-A

150996336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805264-C-G

150996336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805264-C-T

http://identifiers.org/hco/3/GRCh38#150996552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58805448-C-A

150996650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805542-G-A

150996729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805624-T-A

150998652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809490-T-A

150998949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809744-A-G

150999059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809856-T-G

150999090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809886-G-A

150999280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58810084-A-T

150999841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58810779-C-G

150999875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58810813-T-C

150999897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58810835-G-T

150999963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58810901-G-A

151000077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58811030-C-G

151000077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58811030-C-T

151000260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58811181-G-A

151000481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58812976-G-C

151000509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58813006-G-A

151000694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58813180-C-T

151002235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814418-G-A

151002305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814488-A-T

151002369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814552-C-G

151002527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814702-A-G

151002643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814790-C-T

151002676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814823-G-A

151002792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814935-A-G

http://identifiers.org/hco/3/GRCh38#151002820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58814962-C-A

http://identifiers.org/hco/3/GRCh38#151002863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58814972-A-C

151002880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58814989-C-G

151003074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58815181-G-A

151003074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58815181-G-C

151007236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58827110-A-G

151007253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58827127-A-G

151007307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58827178-G-A

151007440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58827300-G-A

151007619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58827503-G-A

http://identifiers.org/hco/3/GRCh38#151008181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58828067-C-A

151008181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828067-C-G

151008491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828388-T-A

151008619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828505-C-T

151008639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828515-A-G

151008708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828585-G-A

151008741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828618-G-A

151008757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828634-A-G

151008810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828686-A-G

151008810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828686-A-T

http://identifiers.org/hco/3/GRCh38#151008901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58828782-A-C

151008922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828802-C-T

151008937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58828816-G-C

151009497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58829294-G-T

http://identifiers.org/hco/3/GRCh38#151009505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58829302-C-A

151009748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58829547-C-T

151009796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58829583-T-C

151009802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58829589-G-A

151010244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58830498-C-G

151010573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58830889-G-A

151010907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831120-G-A

151011298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831309-T-G

151011395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831410-A-G

151011492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831502-G-T

151011515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831524-A-G

151011520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831529-G-A

151011520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831529-G-T

151011604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831606-C-T

151011622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831624-G-A

151011707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831696-G-A

151011750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831739-G-A

151011874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831852-T-C

151011893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58831889-G-A

151012035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58832040-G-A

151012113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58832129-T-C

151012127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58832143-C-T

151012793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58834219-G-A

http://identifiers.org/hco/3/GRCh38#151012827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58834235-C-A

151012892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58834287-C-T

151012969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58834336-A-T

http://identifiers.org/hco/3/GRCh38#151013193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58834558-C-A

151013193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58834558-C-T

151013247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58834607-T-G

151013264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58834621-G-A

151013441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835215-T-C

151013755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835521-T-C

151013771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835537-C-T

151013798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835563-A-G

151013892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835649-T-C

http://identifiers.org/hco/3/GRCh38#151013920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58835676-C-A

151013950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835709-G-A

151013950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835709-G-C

http://identifiers.org/hco/3/GRCh38#151013957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58835716-C-A

151014027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835784-T-C

http://identifiers.org/hco/3/GRCh38#151014061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58835818-C-A

151014129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835886-G-A

151014133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58835890-G-A

151016326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58836760-T-G

151016358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58836801-G-A

http://identifiers.org/hco/3/GRCh38#151016534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58837150-C-A

151016672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58837503-T-C

151016799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58837627-G-A

151016799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58837627-G-C

151016867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58837656-G-A

151017677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58838039-T-C

151017705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58838068-C-T

151017886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58838253-G-A

151017950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58838295-A-G

151020457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58839751-C-G

151020596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58839892-C-G

151021242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58841381-T-C

151021314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58841435-G-T

151021510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58841640-C-T

151021864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58841911-G-A

151021875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58841922-C-T

151021963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842012-T-G

151022017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842067-G-A

http://identifiers.org/hco/3/GRCh38#151022065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58842112-C-A

151022086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842133-T-G

151022256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842341-T-C

151022686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842539-A-G

151022693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842546-T-C

151022726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842579-A-G

151023010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58842870-T-C

151023104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843001-C-T

151023214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843172-A-T

151023266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843241-C-T

151023284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843259-G-C

151023367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843365-A-G

http://identifiers.org/hco/3/GRCh38#151023552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58843609-A-C

151023552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843609-A-G

151023684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843754-A-G

151023687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843757-G-C

151023830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843887-G-C

151023845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58843902-A-G

151024036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58844005-A-G

151024036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58844005-A-T

151024119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58844051-G-C

151024173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58844105-T-C

151024173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58844105-T-G

151024191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58844123-A-G

151027152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58845203-C-G

151027183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58845234-A-G

151027838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58845676-G-A

151027984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58845816-C-T

151028222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58846087-T-C

151029059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58848814-G-A

151029121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58848876-G-A

151029763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849426-T-C

151029870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849534-T-C

151030169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849859-C-T

http://identifiers.org/hco/3/GRCh38#151030171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58849861-C-A

151030171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849861-C-T

151030198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849888-A-G

151030198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849888-A-T

151030274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849964-C-T

151030300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58849990-G-A

http://identifiers.org/hco/3/GRCh38#151030306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58849996-C-A

151030341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58850029-T-C

http://identifiers.org/hco/3/GRCh38#151031562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58850213-A-C

151031912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58850540-C-T

151031932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58850559-T-C

151031987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58850609-T-A

151033003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58850942-T-C

151033103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851041-C-G

151033154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851083-G-A

151033286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851215-C-T

151033330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851257-T-C

151033558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851465-C-T

151033560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851468-C-T

151033731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851636-C-T

151033739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851643-G-A

151033792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58851680-T-C

151037950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58856090-G-A

151037950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58856090-G-C

151038325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58856423-G-A

151038335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58856433-C-T

151038413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58856541-C-G

http://identifiers.org/hco/3/GRCh38#151038491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58856610-C-A

151038591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58856668-T-C

151038746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58856805-C-T

http://identifiers.org/hco/3/GRCh38#151038765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58856825-C-A

http://identifiers.org/hco/3/GRCh38#151038783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58856843-C-A

151038866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58856914-G-A

151038932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58856978-C-T

151040156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58857228-T-C

http://identifiers.org/hco/3/GRCh38#151040183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58857256-A-C

151040245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58857311-T-C

151040290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58857353-C-T

151040305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58857368-G-A

151042518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58857455-C-T

151042629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58857577-A-G

151043059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58857949-T-C

151043275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58858173-C-G

151046433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58864336-G-A

151046553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58864528-G-A

http://identifiers.org/hco/3/GRCh38#151047203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58865668-A-C

151047203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58865668-A-G

151047570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58865976-T-C

151047970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58866471-T-G

151047982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58866503-A-G

151048143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58866656-A-G

http://identifiers.org/hco/3/GRCh38#151048213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58866810-C-A

http://identifiers.org/hco/3/GRCh38#151048291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58866888-C-A

http://identifiers.org/hco/3/GRCh38#151048630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58867208-A-C

151048701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58867281-G-C

151049046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58867605-A-G

151049046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58867605-A-T

151049192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58867705-G-A

http://identifiers.org/hco/3/GRCh38#151049379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58867992-A-C

151049550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58868183-C-T

151049589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58868222-G-A

151049589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58868222-G-C

151049659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58868283-T-C

151049928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58868547-A-T

151050710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

151050734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

151050734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

151050934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/3/GRCh38#151051487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58872542-C-A

151051499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58872554-G-T

151051665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58872730-A-G

151052384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58873014-T-A

151052521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58873156-A-G

151053059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874045-C-G

http://identifiers.org/hco/3/GRCh38#151053078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58874065-A-C

151053217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874197-G-A

151053589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874588-A-G

151053701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874686-G-A

151053701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874686-G-T

151053743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874728-T-C

151053807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874789-A-G

151053824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58874806-G-C

151054141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58875083-T-G

151054168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58875110-C-T

151054260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58875208-T-C

151054352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58880363-A-G

151054386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58880397-T-C

151054494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58880498-C-G

http://identifiers.org/hco/3/GRCh38#151054600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58880614-A-C

151054701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58880711-G-A

151054701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58880711-G-T

151055572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58882176-G-A

151055572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58882176-G-T

151055585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58882189-G-T

http://identifiers.org/hco/3/GRCh38#151056015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58882306-A-C

151056068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58882356-C-T

151056115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58882398-C-T

151056136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58882419-G-A

151056152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58882435-A-G

151057028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58884447-T-C

151057028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58884447-T-G

151057156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58884578-C-G

151057401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58884808-C-T

151057427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58884837-A-G

http://identifiers.org/hco/3/GRCh38#151057884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58885238-C-A

151060205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58885465-G-A

151060233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58885494-T-C

151060255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58885515-G-A

151060374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58885630-G-A

151060374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58885630-G-C

151060662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58885956-C-G

151060682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58885976-T-C

151060767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58886530-T-C

http://identifiers.org/hco/3/GRCh38#151060784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58886547-A-C

151060784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58886547-A-G

151062853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58888298-T-C

151062875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58888317-C-G

151062875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58888317-C-T

http://identifiers.org/hco/3/GRCh38#151063334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58889010-A-C

151063704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58889414-A-G

151072042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58892131-T-C

151072160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58892249-A-G

151072186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58892292-T-C

151072302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58892414-G-A

151072302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58892414-G-T

151072395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58892535-G-A

151073820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58895981-T-A

http://identifiers.org/hco/3/GRCh38#151074506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58897035-C-A

http://identifiers.org/hco/3/GRCh38#151075010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58897662-C-A

151075010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58897662-C-T

151075172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58897952-G-A

151075353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58898114-G-T

http://identifiers.org/hco/3/GRCh38#151075358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58898119-A-C

151075358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58898119-A-G

http://identifiers.org/hco/3/GRCh38#151075375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58898136-C-A

151075963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58899339-T-G

151076479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58899838-C-G

151076570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58899924-A-G

151076637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58899991-A-G

151076987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58900398-A-G

151077052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58900482-T-G

151077912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58904650-A-G

151078890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 58907824-A-G

151078890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 58907824-A-T

151078917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58907852-G-A

151078932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58907867-T-C

151079030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58907943-A-G

151079317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58908855-G-T

151079408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58908921-G-A

151079555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58909090-G-T

151079562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58909094-T-C

151079587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58909117-G-T

151080720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30895
most severe consequence: non coding transcript exon variant
orthologous variants: 58910427-C-T