131904123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65658920-T-A

131904123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65658920-T-C

131904225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65658994-G-A

131904225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65658994-G-C

131904225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65658994-G-T

131904236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65659005-G-A

131904236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65659005-G-C

131904236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65659005-G-T

131904845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65659436-A-G

131905028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65659582-G-C

131906139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65660498-A-G

http://identifiers.org/hco/8/GRCh38#131906454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65660789-A-C

131906454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65660789-A-G

131906750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65661050-G-T

131906801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65661089-A-G

131907348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65661742-A-T

http://identifiers.org/hco/8/GRCh38#131907700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65662045-A-C

131907893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65662930-T-G

131908009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663221-G-A

131908064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663274-T-C

131908085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663295-G-T

131909635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663491-A-G

131909692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663543-G-A

131910038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663949-T-A

131910093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65664006-T-C

http://identifiers.org/hco/8/GRCh38#131910122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65664030-A-C

131910122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65664030-A-G

131910124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65664032-A-G

131910256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65664118-A-T

131910259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65664121-A-G

131910639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65664249-C-T

131910755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65664326-C-G

131912249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65665330-A-G

131912249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65665330-A-T

131912604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65666243-C-G

131912677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65667406-A-G

http://identifiers.org/hco/8/GRCh38#131912976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65667653-C-A

131912979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65667656-G-T

131913220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65667856-C-T

131913225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65667861-A-G

131913506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668108-A-G

131913629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668219-T-C

131913709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668282-G-A

131913709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668282-G-C

131913851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668424-A-T

131913937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668523-G-A

131913937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668523-G-T

131914553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65669057-A-G

131914562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65669066-G-A

131915491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65669505-C-G

131915573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65669581-G-A

131917122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65670567-T-C

131917335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65670772-C-G

131917396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65670825-A-G

131917426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65670863-C-T

131917556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65670981-A-G

131917603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65671027-C-T

131917864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65671256-G-A

131918589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65673781-A-G

131918720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65673901-T-C

131918875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65674053-G-C

131919047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65674249-C-T

131919099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65674301-A-T

131919118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65674328-G-T

131919867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65674659-T-C

131920649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65675408-C-T

http://identifiers.org/hco/8/GRCh38#131921010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65675717-C-A

131921285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65675947-A-G

131921664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65676295-G-A

131922122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65676667-G-A

131932706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65677713-A-T

131932752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65677759-T-C

131933028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678033-A-G

131933185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678221-A-T

131933234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678309-G-A

131933445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678527-G-A

131933727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678803-T-G

131933737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678812-A-G

131933740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678815-G-T

131933861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65678947-G-C

131934026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679107-G-C

131934153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679235-T-A

131934154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679236-A-G

131934164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679242-T-C

131934187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679265-C-T

131934285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679359-C-T

131934349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679410-C-T

131934404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679465-C-T

131934515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679572-A-G

131934841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65679713-G-A

131935219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680027-A-G

131935372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680185-A-G

131935397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680210-G-T

131935400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680213-A-G

131935416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680227-G-A

131935511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680304-A-G

131935548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680944-T-C

http://identifiers.org/hco/8/GRCh38#131935556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65680952-C-A

131935556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65680952-C-T

131937742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65681631-A-G

131938032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65681898-T-C

131938059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65681925-A-G

131938183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682046-T-C

131938242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65682100-G-C

131938302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65682160-A-G

131938340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682198-T-G

131938361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682272-G-T

131938377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682289-T-G

131938394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682331-A-G

131938404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682341-G-T

131938448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682387-A-G

131938612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682553-A-G

131938613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682554-T-C

131938785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682687-C-T

131938869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682759-G-C

131938897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682782-T-C

131938968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682854-A-G

131939104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682985-C-T

131939449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65683270-A-G

131939653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65683418-T-A

131939744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65683492-G-T

131939749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65683497-T-C

131939751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65683499-T-C

http://identifiers.org/hco/8/GRCh38#131939761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65683514-A-C

131940419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65687109-A-T

131940432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65687122-T-G

http://identifiers.org/hco/8/GRCh38#131940445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65687135-C-A

131940445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65687135-C-T

131940560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65687245-C-T

131940690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65687370-T-G

131940899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65687525-A-G

131941196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65687838-A-G

131941281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65688445-T-C

131941290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65688454-G-A

131941390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65688533-A-G

131941410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65688547-C-T

131941633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65688779-T-A

131941918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689039-T-C

131942259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689343-G-C

131942259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689343-G-T

131942582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689616-C-G

131942608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689647-G-A

131942639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689676-G-C

131944457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689982-C-T

131944546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690075-G-A

131944599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690132-G-A

131944599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690132-G-T

131944617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690150-G-A

131944617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690150-G-T

131944720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690262-C-T

131944742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65690279-T-C

131944898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690431-T-C

http://identifiers.org/hco/8/GRCh38#131945020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65690560-A-C

131945020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690560-A-G

131945054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690590-C-T

131945121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690657-A-G

131946139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691298-A-T

131946258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691415-G-A

http://identifiers.org/hco/8/GRCh38#131946406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65691495-A-C

131946467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691540-T-C

131946492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65691578-G-A

131946492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65691578-G-C

131946492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65691578-G-T

131946504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65691590-G-A

131946507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65691593-A-G

131946507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65691593-A-T

131946742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691825-T-G

131946763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691846-A-G

131946769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691852-A-T

131946771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691854-T-A

131946771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691854-T-G

131946793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65691873-T-C

131947440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65692377-T-C

131947751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65692623-C-T

131947907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65692742-T-G

131948106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65692919-T-G

131948388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65693505-C-G

131948629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65693760-G-T

131948829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65693955-G-T

131949031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65694374-A-G

131949116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65694451-T-C

131949844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65696330-T-C

131949844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65696330-T-G

http://identifiers.org/hco/8/GRCh38#131949903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65696395-A-C

131950152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65696655-A-G

131950152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65696655-A-T

131950286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65696774-C-T

131952337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65700410-C-T

131952402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65700479-C-T

131952443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65700517-G-A

131952459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65700533-C-G

131952627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65700649-A-G

131952773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65700761-A-G

131952849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65700837-C-T

131952946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65700917-G-A

131953105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701063-T-C

131953105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701063-T-G

131953696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701465-T-G

http://identifiers.org/hco/8/GRCh38#131953798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65701564-C-A

131953798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701564-C-T

131953884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65701642-G-A

131953884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65701642-G-T

131953935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65701693-G-A

131953935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65701693-G-C

131953935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65701693-G-T

http://identifiers.org/hco/8/GRCh38#131953980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65701733-A-C

131953980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701733-A-T

131953983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701736-T-A

131953983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701736-T-C

131953989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701742-T-A

131953989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65701742-T-C

http://identifiers.org/hco/8/GRCh38#131954003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65706358-C-A

131954003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706358-C-G

131954003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706358-C-T

131954016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706370-G-T

131954033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706387-G-T

131954042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706396-G-T

131954098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706452-A-G

131954100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706454-A-G

http://identifiers.org/hco/8/GRCh38#131954105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65706459-C-A

131954155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706519-C-G

131954374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706752-A-T

131954383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65706761-A-G

131955613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709123-G-T

http://identifiers.org/hco/8/GRCh38#131955642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65709156-C-A

131955642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709156-C-G

131955656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709170-G-A

131955656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709170-G-T

131955702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709218-A-G

131955859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65709375-C-G

131955859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 65709375-C-T

131955921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709437-T-C

131956052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709465-A-G

131956128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709512-G-C

131956161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709539-G-C

131956375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709776-A-G

131956501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709899-C-T

131956577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65709980-A-G

131956602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65710005-G-T

131956653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65710051-A-T

131956775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65710170-T-C

131957238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65711679-G-A

131957298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65711727-A-G

131957301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65711730-A-G

http://identifiers.org/hco/8/GRCh38#131957316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65711745-A-C

131957316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65711745-A-G

131957836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65711940-A-G

131958100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65712223-C-T

131959757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65714656-A-T

131966953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65715196-C-T

131966991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65715236-A-G

http://identifiers.org/hco/8/GRCh38#131967060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65715304-C-A

131967069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65715308-G-C

131967838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65716993-T-C

131967842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65716997-A-G

131967843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65716998-T-C

http://identifiers.org/hco/8/GRCh38#131967859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65717012-A-C

131967954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65717103-A-G

131968060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65717562-T-C

131968119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65717617-G-A

131968152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65717646-G-A

131968152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65717646-G-T

http://identifiers.org/hco/8/GRCh38#131968237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65717728-A-C

131968514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65717955-T-C

131968514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65717955-T-G

131969626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65719243-T-C

131969726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65719342-G-T

131969825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65719435-G-A

131970075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65719627-T-C

http://identifiers.org/hco/8/GRCh38#131970121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65719668-C-A

131970283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65719829-G-T

http://identifiers.org/hco/8/GRCh38#131970323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65719862-C-A

131970359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65719902-T-G

131970574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65720095-G-A

http://identifiers.org/hco/8/GRCh38#131970691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65720205-C-A

131970714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65720232-G-T

131970736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65720254-A-G

131970738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65720259-G-T

131975968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65721556-G-A

131975987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65721575-A-G

131976153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65721738-G-C

131976153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65721738-G-T

131976380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65721948-G-T

http://identifiers.org/hco/8/GRCh38#131976471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65722032-A-C

131976471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722032-A-G

131976746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722520-G-A

131976746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722520-G-T

http://identifiers.org/hco/8/GRCh38#131976800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65722618-C-A

131976800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722618-C-T

131976810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722628-A-G

131976863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722787-A-G

131976991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65722923-G-A

131977171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723097-A-G

131977171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723097-A-T

131977178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723104-T-C

131977178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723104-T-G

131977193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723119-A-G

131977308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723240-A-G

131977370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723315-G-A

131977398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65723340-C-G

131978501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65724473-A-G

131978741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65724697-G-A

131978741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65724697-G-T

131978811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65724770-T-A

131978811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65724770-T-C

131978873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65724836-G-A

131978873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65724836-G-T

131978888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65724851-G-A

131978888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65724851-G-T

131979099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725068-A-T

131979111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725081-T-C

131979291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725325-T-C

http://identifiers.org/hco/8/GRCh38#131979458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65725479-A-C

131979458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725479-A-G

131979513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65725531-T-A

131984153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65726492-G-A

131984326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726665-A-G

131984328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726667-A-T

131984362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726703-A-G

131984548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726827-C-T

131984596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726875-A-G

131984603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726882-A-G

131984628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726907-C-G

131984628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726907-C-T

131984721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65726974-C-T

131984979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65727315-A-G

http://identifiers.org/hco/8/GRCh38#131985108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65727444-C-A

131985165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727540-G-T

131985265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727610-G-A

131985421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727707-G-C

131985515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727788-T-C

131985684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727936-T-A

131985747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65727981-C-T

131985980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728184-C-T

131986279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728456-A-G

131986279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728456-A-T

http://identifiers.org/hco/8/GRCh38#131986311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65728490-C-A

131986815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728646-G-A

131986913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728739-C-T

131986919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728746-C-G

131987113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728919-C-G

131987196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65728998-A-G

131987296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729092-C-G

http://identifiers.org/hco/8/GRCh38#131987461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65729208-C-A

131987461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729208-C-G

http://identifiers.org/hco/8/GRCh38#131987497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65729236-C-A

131987497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729236-C-T

131987498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729237-T-A

http://identifiers.org/hco/8/GRCh38#131987528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65729267-C-A

131987528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729267-C-T

131987549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729287-G-A

131987549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729287-G-T

131988789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65729846-A-G

131989048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730085-G-T

131989128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730169-T-C

131989266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730306-A-G

131989603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730656-A-T

131989730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730817-G-A

131989749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730835-A-G

131989759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65730845-A-G

131990003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731030-C-T

131990152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731147-A-G

131994597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731642-A-G

131994995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65731983-T-G

131995173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732166-T-C

131995206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732189-A-T

131995339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732313-A-G

131995359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65732334-C-T

131996219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733318-T-G

http://identifiers.org/hco/8/GRCh38#131996335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65733436-A-C

131996335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733436-A-T

http://identifiers.org/hco/8/GRCh38#131996506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65733601-C-A

http://identifiers.org/hco/8/GRCh38#131996605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65733700-C-A

131996607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733702-T-A

131996607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733702-T-G

131996724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65733791-G-T

131996997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734065-G-T

131997066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734127-T-C

131997156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734217-A-G

131997157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65734218-C-T

http://identifiers.org/hco/8/GRCh38#131997657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65735728-C-A

132000675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65736422-A-G

132000989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65736731-A-G

132001084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65736827-G-A

132001354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65737361-C-T

132001695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65737667-A-T

132001770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65737738-T-C

132002036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65737959-T-C

132002211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738118-A-G

132002597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65738567-G-A

132002795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738745-T-C

132002853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738778-A-G

132002896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738820-A-T

132002928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738845-G-A

132002939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65738856-T-C

132003232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65739115-G-A

132003232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65739115-G-T

132003425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739269-T-A

132003597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739429-T-C

132003609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739441-T-C

132003625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739457-G-A

132003686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739500-A-G

132003699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739513-T-G

132003883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65739705-T-C

132008928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741265-G-A

http://identifiers.org/hco/8/GRCh38#132008983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65741323-C-A

132008999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741337-T-C

http://identifiers.org/hco/8/GRCh38#132009045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65741383-C-A

132009045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65741383-C-T

132010110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742482-T-C

http://identifiers.org/hco/8/GRCh38#132010644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65742879-C-A

132010644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742879-C-T

132010688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65742922-A-T

132010851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65743063-G-A

132011009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743221-A-G

132011052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743262-T-C

132011052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743262-T-G

132011095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743301-G-A

132011116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743321-G-T

132011139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743344-A-G

132011150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743355-G-T

132011212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743414-A-G

132011212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743414-A-T

http://identifiers.org/hco/8/GRCh38#132011421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65743581-A-C

132011476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743634-G-A

132011479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743637-G-T

132011588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743738-G-A

132011688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743835-C-T

132011745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743894-A-G

132011757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743906-G-A

132011813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65743963-A-G

http://identifiers.org/hco/8/GRCh38#132012003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65744147-A-C

132012109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65744221-G-A

132012222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65744333-G-T

http://identifiers.org/hco/8/GRCh38#132012289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65744400-C-A

132012326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65744456-A-G

http://identifiers.org/hco/8/GRCh38#132012362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65744493-C-A

132012467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65744592-C-G

132012555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65744670-G-A

http://identifiers.org/hco/8/GRCh38#132012567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65744683-C-A

132012567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65744683-C-G

132013023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65745121-A-G

http://identifiers.org/hco/8/GRCh38#132013320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28970
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#65745402-C-A