70454730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111629004-G-T

70454775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111628971-G-T

70454777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111628969-G-A

70454796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111628950-G-C

70454821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111628934-C-T

http://identifiers.org/hco/16/GRCh38#70454857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111628898-C-A

70454857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111628898-C-T

70454903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111628871-A-G

70454959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111628834-G-A

http://identifiers.org/hco/16/GRCh38#70463093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111626642-A-C

70463106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626630-A-G

70463218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111626517-A-G

http://identifiers.org/hco/16/GRCh38#70463344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111626389-C-A

70463344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626389-C-T

70463512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626277-G-A

70463512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626277-G-T

70463594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626207-G-C

70463594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626207-G-T

http://identifiers.org/hco/16/GRCh38#70463595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111626206-C-A

70463595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626206-C-T

70463598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626203-G-A

70463598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626203-G-T

70463652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111626147-A-T

70463658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111626141-G-C

70463697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111626102-C-T

http://identifiers.org/hco/16/GRCh38#70463811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111625985-C-A

70463811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625985-C-T

70465121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111625885-T-C

70465305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625685-A-G

70466122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622652-C-T

70466303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111622468-A-G

70466363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111622402-G-T

http://identifiers.org/hco/16/GRCh38#70466482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111622300-C-A

70466482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111622300-C-T

70466493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111622289-G-A

70466493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111622289-G-T

http://identifiers.org/hco/16/GRCh38#70466506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111622276-A-C

70466507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111622275-A-G

70466549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622237-T-A

70466549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622237-T-C

70466549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622237-T-G

70466601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622220-G-A

70466601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622220-G-T

70466609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622207-A-T

http://identifiers.org/hco/16/GRCh38#70466611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111622205-C-A

70466611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622205-C-T

70466731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622117-A-G

70466731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622117-A-T

70466764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622096-G-A

70466764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622096-G-T

70466769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622091-A-T

70466777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622083-T-C

70466814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111622052-G-T

70466972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621883-T-C

70467001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621851-G-A

70467001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621851-G-C

70467001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621851-G-T

70467006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621834-A-G

http://identifiers.org/hco/16/GRCh38#70467019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621819-C-A

70467019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621819-C-T

70467046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621796-T-G

70467047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621795-G-A

70467047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621795-G-C

70467047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621795-G-T

70467142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621670-A-G

70467148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621664-T-C

70467165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621647-G-A

70467165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621647-G-T

70467175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621638-T-A

70467175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621638-T-C

http://identifiers.org/hco/16/GRCh38#70467185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621628-C-A

70467185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621628-C-T

http://identifiers.org/hco/16/GRCh38#70467238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621572-C-A

70467253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621556-C-T

http://identifiers.org/hco/16/GRCh38#70467277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621533-C-A

70467277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621533-C-T

70467303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621509-T-A

70467317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621495-G-A

70467317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111621495-G-T

70467409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111621421-A-G

70467436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111621394-G-A

70467436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111621394-G-T

http://identifiers.org/hco/16/GRCh38#70467437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621393-C-A

70467437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111621393-C-G

70467437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111621393-C-T

70467454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111621376-T-C

http://identifiers.org/hco/16/GRCh38#70467573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621267-C-A

70467573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621267-C-G

70467573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621267-C-T

70467680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621206-C-T

http://identifiers.org/hco/16/GRCh38#70467687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621199-A-C

70467687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621199-A-G

70467755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621107-A-G

70467755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621107-A-T

70467764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621098-A-G

70467764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621098-A-T

70467768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621094-G-A

70467768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621094-G-T

http://identifiers.org/hco/16/GRCh38#70467785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111621075-A-C

70467785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111621075-A-T

70467934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111620928-C-T

http://identifiers.org/hco/16/GRCh38#70467943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111620919-A-C

http://identifiers.org/hco/16/GRCh38#70467962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111620900-C-A

70467962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111620900-C-T

70468056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620794-C-G

70468056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620794-C-T

70468742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620493-G-C

70468742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620493-G-T

70468762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620473-G-A

70468762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620473-G-T

70468782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620453-C-G

70468782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620453-C-T

70468813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620421-G-A

70468813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620421-G-T

70468852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111620385-T-C

70468858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111620379-G-A

70468986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620252-G-C

70468986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620252-G-T

70468994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620245-G-T

70468998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620241-C-T

70469003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620236-T-C

70469036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620203-C-T

70469050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620189-T-G

70469081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620160-T-C

70469089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620152-C-T

70469129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620112-T-C

70469130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620111-G-A

70469130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111620111-G-T

70469213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 111620029-T-A

70469213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 111620029-T-C

70469333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111619909-G-C

70469333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111619909-G-T

70469430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111619835-T-A

70469488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111619780-T-C

70469504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111619764-C-G

70469504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111619764-C-T

70470232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111618893-A-G

http://identifiers.org/hco/16/GRCh38#70470452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111618661-C-A

70470452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111618661-C-T

70470537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111618379-G-A

70470537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111618379-G-T

70470885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111617287-T-C

70470886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111617286-T-C

http://identifiers.org/hco/16/GRCh38#70470943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111617225-C-A

70470943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111617225-C-G

70470943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111617225-C-T

70470998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111617172-T-A

http://identifiers.org/hco/16/GRCh38#70471016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#111617154-C-A

70471016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111617154-C-G

70471016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 111617154-C-T

70471073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 111617097-G-A

70471073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 111617097-G-T

http://identifiers.org/hco/16/GRCh38#70471085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#111617085-C-A

70471085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111617085-C-T

70471108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111617051-G-A

70471108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111617051-G-T

70471138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111617023-T-G

70471141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111617020-G-A

70471141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111617020-G-T

70471160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616997-T-G

70471266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111616892-G-T

http://identifiers.org/hco/16/GRCh38#70471267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111616891-A-C

http://identifiers.org/hco/16/GRCh38#70471314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111616844-C-A

70471314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111616844-C-G

70471314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111616844-C-T

70471390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616768-A-G

70471471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616689-G-A

70471471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616689-G-T

http://identifiers.org/hco/16/GRCh38#70472474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111616439-C-A

70472474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616439-C-T

70472645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616261-G-A

70472645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616261-G-T

70472834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616067-A-G

70472870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616026-G-A

70472870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616026-G-T

70472889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111616006-T-C

http://identifiers.org/hco/16/GRCh38#70472896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615999-C-A

70472896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615999-C-G

70472896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615999-C-T

70472962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615939-T-A

70472962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615939-T-C

70472965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615936-G-A

70472965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615936-G-T

70473013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111615889-G-A

70473013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111615889-G-C

70473013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111615889-G-T

http://identifiers.org/hco/16/GRCh38#70473034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615868-C-A

70473040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111615862-C-T

http://identifiers.org/hco/16/GRCh38#70473101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615801-C-A

70473101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111615801-C-T

http://identifiers.org/hco/16/GRCh38#70473109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615793-C-A

http://identifiers.org/hco/16/GRCh38#70473131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615771-C-A

70473131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111615771-C-G

70473131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111615771-C-T

http://identifiers.org/hco/16/GRCh38#70473155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615747-C-A

70473155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111615747-C-G

70473155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111615747-C-T

70473287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111615615-C-T

70473302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111615600-G-A

70473302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111615600-G-C

70473302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111615600-G-T

70473393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615507-G-A

70473393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615507-G-T

70473448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615445-G-A

70473448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615445-G-T

http://identifiers.org/hco/16/GRCh38#70473471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615426-C-A

70473471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615426-C-T

http://identifiers.org/hco/16/GRCh38#70473475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111615422-C-A

70473653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615289-T-C

70473670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615260-G-A

70473677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615253-C-T

70473856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615105-G-A

70473870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111615091-A-G

70473985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614705-A-G

http://identifiers.org/hco/16/GRCh38#70473994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111614696-C-A

70474005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614650-T-A

70474005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614650-T-G

70474006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614649-G-A

70474006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614649-G-T

70474009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614622-G-T

70474010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614621-G-A

70474010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614621-G-T

70474026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614605-G-A

70474026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614605-G-T

70474034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614597-T-A

70474063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614571-C-G

70474063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614571-C-T

70474311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111614326-G-A

70474311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111614326-G-C

70474487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614186-T-C

http://identifiers.org/hco/16/GRCh38#70474508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111614165-C-A

70474508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111614165-C-G

http://identifiers.org/hco/16/GRCh38#70474629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111614050-A-C

70474631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111614048-G-A

70474634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111614045-G-A

70474634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 111614045-G-T

70474893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111613799-C-G

http://identifiers.org/hco/16/GRCh38#70475002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111613690-C-A

70475002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111613690-C-G

70475002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111613690-C-T

70475045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613638-G-A

70475045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613638-G-T

70475208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613450-G-T

70475273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613399-T-C

70475275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613397-G-C

70475275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613397-G-T

70475296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613367-G-A

70475296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613367-G-T

70475333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613330-T-C

70475341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613325-C-G

70475341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613325-C-T

70475385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111613281-A-G

70475454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111613212-C-T

http://identifiers.org/hco/16/GRCh38#70475475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111613191-C-A

70475475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111613191-C-G

70475475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111613191-C-T

http://identifiers.org/hco/16/GRCh38#70475503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111613167-C-A

70475503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613167-C-T

http://identifiers.org/hco/16/GRCh38#70475596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111613095-C-A

70475596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613095-C-G

70475596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111613095-C-T

70475643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111613047-T-C

70475701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111612989-G-C

70475753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111612937-A-G

70475770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111612920-A-G

70476041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612768-C-G

70476041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612768-C-T

http://identifiers.org/hco/16/GRCh38#70476383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111612529-C-A

70476383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612529-C-T

70476390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612521-G-A

70476390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612521-G-C

70476394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612517-T-C

70476395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612516-G-A

70476395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612516-G-T

70476401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612509-G-A

70476401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612509-G-T

70476417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612493-T-A

70476417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612493-T-C

http://identifiers.org/hco/16/GRCh38#70476446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111612472-C-A

70476446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612472-C-T

70476483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612443-G-A

70476483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612443-G-T

70476553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612381-G-T

70476630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612308-T-C

70476912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111612003-C-T

70477003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111611939-G-A

70477255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111611631-C-T

http://identifiers.org/hco/16/GRCh38#70477264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111611622-C-A

70477264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111611622-C-G

70477264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111611622-C-T

70477279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111611608-T-C

70477320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111611575-T-C

70477372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611509-T-A

70477372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611509-T-C

70477389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611488-G-A

70477432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611450-T-A

70477432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611450-T-C

70477440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611442-C-T

70477462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611421-G-A

70477462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611421-G-T

70477469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611414-A-G

70477469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611414-A-T

http://identifiers.org/hco/16/GRCh38#70477470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111611413-C-A

70477470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611413-C-T

70477472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611411-A-G

70477473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611410-T-C

70477478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611405-G-A

70477478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611405-G-T

70478039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611035-G-A

70478039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111611035-G-T

http://identifiers.org/hco/16/GRCh38#70478049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111611025-A-C

http://identifiers.org/hco/16/GRCh38#70478196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111610921-C-A

70478196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111610921-C-T

70478512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111610607-C-T

70478530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111610590-C-T

70478664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111610457-T-C

70478664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111610457-T-G

70478758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111610407-G-A

70478865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610322-T-C

70478901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610286-G-A

70478901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610286-G-C

70478901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610286-G-T

70478940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610249-A-G

70478973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610228-T-A

70478989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610213-T-G

70478998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111610204-T-G

http://identifiers.org/hco/16/GRCh38#70479012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111610193-C-A

http://identifiers.org/hco/16/GRCh38#70479295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609966-C-A

70479295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111609966-C-T

http://identifiers.org/hco/16/GRCh38#70479462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609802-C-A

70479462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111609802-C-T

70479493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111609788-G-A

70479493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111609788-G-T

http://identifiers.org/hco/16/GRCh38#70479495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609786-C-A

70479495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111609786-C-G

http://identifiers.org/hco/16/GRCh38#70479648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609647-A-C

http://identifiers.org/hco/16/GRCh38#70479699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609612-A-C

70479699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609612-A-G

70479729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609586-C-T

70479746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609572-T-C

70479746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609572-T-G

70479760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609560-T-C

http://identifiers.org/hco/16/GRCh38#70479768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609552-C-A

70479768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609552-C-T

70479788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609532-T-C

70479810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609517-G-T

http://identifiers.org/hco/16/GRCh38#70479855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609468-C-A

70479855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609468-C-T

70479863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609460-A-G

http://identifiers.org/hco/16/GRCh38#70479884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609439-C-A

70479929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609394-T-C

http://identifiers.org/hco/16/GRCh38#70479932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609391-C-A

70479932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609391-C-G

http://identifiers.org/hco/16/GRCh38#70479943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609380-C-A

70479945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609378-T-C

http://identifiers.org/hco/16/GRCh38#70480035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609323-C-A

http://identifiers.org/hco/16/GRCh38#70480091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111609290-C-A

70480156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609224-T-G

70480161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609219-T-C

70480161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609219-T-G

70480222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609146-G-A

70480229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609139-G-A

70480229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609139-G-C

70480229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609139-G-T

70480239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29500
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111609129-C-T