http://identifiers.org/hco/10/GRCh38#71747569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60208979-C-A

71747615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60208943-A-G

71747627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60208931-G-T

71747668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60208124-G-A

http://identifiers.org/hco/10/GRCh38#71747763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60208036-C-A

http://identifiers.org/hco/10/GRCh38#71747819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207980-C-A

71747819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 60207980-C-G

71748000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207612-A-G

http://identifiers.org/hco/10/GRCh38#71748081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207512-C-A

71748105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207488-G-T

71748154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207409-G-A

71748179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207388-C-T

http://identifiers.org/hco/10/GRCh38#71748182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207385-C-A

71748182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207385-C-T

http://identifiers.org/hco/10/GRCh38#71748183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207384-C-A

http://identifiers.org/hco/10/GRCh38#71748186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207381-C-A

71748186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207381-C-T

http://identifiers.org/hco/10/GRCh38#71748212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207356-A-C

http://identifiers.org/hco/10/GRCh38#71748213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207355-C-A

71748213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 60207355-C-T

http://identifiers.org/hco/10/GRCh38#71748231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207341-C-A

71748231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207341-C-T

http://identifiers.org/hco/10/GRCh38#71748260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207298-C-A

71748260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207298-C-T

http://identifiers.org/hco/10/GRCh38#71748365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207221-C-A

71748365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207221-C-T

http://identifiers.org/hco/10/GRCh38#71748382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207208-C-A

71748382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207208-C-T

http://identifiers.org/hco/10/GRCh38#71748394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207196-C-A

71748394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207196-C-T

http://identifiers.org/hco/10/GRCh38#71748460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#60207145-A-C

71748460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 60207145-A-G

71748587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60207037-T-C

71748755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206884-G-A

71748755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206884-G-T

http://identifiers.org/hco/10/GRCh38#71748760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60206879-C-A

71748760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206879-C-T

http://identifiers.org/hco/10/GRCh38#71748835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60206814-C-A

71749172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206501-T-C

http://identifiers.org/hco/10/GRCh38#71749423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60206435-C-A

71749448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206426-A-G

71749561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206321-A-G

71749587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206297-G-A

http://identifiers.org/hco/10/GRCh38#71749589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60206295-C-A

71749780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60206163-G-T

http://identifiers.org/hco/10/GRCh38#71749961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60205982-C-A

71749961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205982-C-T

http://identifiers.org/hco/10/GRCh38#71749991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60205951-C-A

71749991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205951-C-T

71750063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205892-C-T

http://identifiers.org/hco/10/GRCh38#71750074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60205885-C-A

http://identifiers.org/hco/10/GRCh38#71750158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60205830-C-A

71750267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205726-A-G

71750270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205723-A-G

71750390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205545-G-T

71750425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205503-G-T

71750428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205500-A-G

71750428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205500-A-T

71750431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205497-A-T

71750439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205489-G-A

71750439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205489-G-T

71750487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205442-C-T

http://identifiers.org/hco/10/GRCh38#71750488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60205441-C-A

71750562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205387-A-G

71750617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205325-A-G

71750619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205323-G-A

71750619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205323-G-C

71750619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205323-G-T

71750621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205321-T-C

71750627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205315-G-A

71750627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205315-G-T

71750655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205288-G-C

http://identifiers.org/hco/10/GRCh38#71750782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60205175-C-A

71750782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205175-C-G

71750782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205175-C-T

71750826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205127-G-A

71750826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205127-G-T

71750860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205097-G-A

http://identifiers.org/hco/10/GRCh38#71750863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60205094-C-A

71750863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205094-C-T

71750898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60205059-T-C

71751001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204978-G-A

71751001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204978-G-T

http://identifiers.org/hco/10/GRCh38#71751009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60204971-C-A

71751009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204971-C-T

http://identifiers.org/hco/10/GRCh38#71751068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60204915-C-A

71751068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204915-C-T

71751103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204864-G-A

71751103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204864-G-T

71751108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204859-G-T

71751126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204845-T-C

http://identifiers.org/hco/10/GRCh38#71751207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60204762-A-C

71751232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204737-G-A

71751232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60204737-G-C

http://identifiers.org/hco/10/GRCh38#71751392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60204637-C-A

71751398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204631-G-C

71751651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204520-G-T

http://identifiers.org/hco/10/GRCh38#71751925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60204249-C-A

71751925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204249-C-T

71752001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204201-G-A

71752001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204201-G-T

71752071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204153-A-G

71752150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204144-C-G

71752150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204144-C-T

http://identifiers.org/hco/10/GRCh38#71752206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60204119-A-C

71752206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60204119-A-G

71752360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60203997-C-T

71753113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60203484-G-T

71753176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60203446-G-A

71753207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60203418-G-A

http://identifiers.org/hco/10/GRCh38#71753689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60203102-C-A

http://identifiers.org/hco/10/GRCh38#71753799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60202968-A-C

71753976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60202834-G-C

71755132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60200253-T-C

71755181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60200208-T-A

71755181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60200208-T-G

71755247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60200159-A-G

71755247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60200159-A-T

71755489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199957-A-G

71755489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199957-A-T

71755491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199955-G-A

71755491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199955-G-C

71755509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199936-T-C

71755607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199675-T-C

http://identifiers.org/hco/10/GRCh38#71755673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60199616-C-A

71755699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199590-T-C

71755699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199590-T-G

71755730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199559-G-A

71755831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60199476-T-C

71756900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60197927-A-G

http://identifiers.org/hco/10/GRCh38#71756913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60197922-A-C

http://identifiers.org/hco/10/GRCh38#71757442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60197447-C-A

71757483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60197406-A-G

71757490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60197400-A-G

http://identifiers.org/hco/10/GRCh38#71757492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60197398-C-A

71757492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60197398-C-T

71757583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60197335-A-G

71757725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60197198-G-A

71757725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60197198-G-T

71757885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60197094-C-T

71760818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60194830-G-T

71760848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60194800-G-C

71760848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60194800-G-T

71760973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60194673-G-T

71761036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60194608-T-A

71761047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60194597-G-T

71761084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60194532-C-T

http://identifiers.org/hco/10/GRCh38#71761101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60194487-A-C

71761258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60194346-C-G

http://identifiers.org/hco/10/GRCh38#71761452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60194166-C-A

71761452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60194166-C-T

71761505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60194125-C-T

http://identifiers.org/hco/10/GRCh38#71761527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60194103-C-A

71761699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60193943-G-A

71761706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60193936-T-G

71761714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60193928-G-A

71761782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60193860-G-A

http://identifiers.org/hco/10/GRCh38#71761804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60193838-C-A

71761804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60193838-C-T

71761905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60193740-G-A

http://identifiers.org/hco/10/GRCh38#71762046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60193598-C-A

http://identifiers.org/hco/10/GRCh38#71762076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60193568-C-A

71762076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60193568-C-T

71762087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60193557-A-G

http://identifiers.org/hco/10/GRCh38#71762102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60193538-C-A

71762104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60193536-T-A

71762118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60193523-T-C

71762118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60193523-T-G

71762400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60193262-G-A

71762769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60192914-C-T

71762811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60192870-T-C

71762920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60192780-A-G

71763701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60191175-T-C

71764019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60190904-T-C

71764135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60190792-C-G

71764182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60190755-C-T

71764983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60190170-C-T

71765016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60190136-T-C

71765064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60190091-G-A

71765292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189902-A-G

71765408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189810-A-G

71765450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189801-G-T

71765659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60189627-C-G

71765713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189573-C-G

71765713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189573-C-T

71765979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189409-G-A

71766066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189316-G-A

71766110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189255-A-G

71766238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189127-C-T

http://identifiers.org/hco/10/GRCh38#71766353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60189028-C-A

71766353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189028-C-T

71766354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60189027-C-T

71766406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60188978-G-A

71766523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60188862-G-A

http://identifiers.org/hco/10/GRCh38#71766533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60188852-A-C

71766869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60188107-T-C

71766950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60188027-C-T

71767455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60187611-C-G

71767479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60187586-G-A

71767605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60187485-A-G

71767647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60187435-T-C

71767694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60187403-G-A

71767720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60187379-G-A

71767777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60187322-C-T

71768996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60186806-T-C

71769402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60186426-G-T

71769597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60186227-G-C

71769620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60186206-C-T

71769706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, undefined
orthologous variants: 60186125-C-T

71770161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60185706-T-C

71770276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60185598-C-T

71770371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60185515-G-A

71771071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60184930-C-T

http://identifiers.org/hco/10/GRCh38#71771102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#60184914-C-A

71771769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60184355-T-C

71772346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60183817-C-T

71772521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60183608-C-T

71772696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60183483-A-G

71772772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60183406-T-C

71773117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60183093-T-C

71773239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60182996-T-A

71773239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60182996-T-C

71773239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60182996-T-G

71773257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron variant
orthologous variants: 60182978-A-G

71773386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 60182852-G-A

71773386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 60182852-G-T

71773471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60182758-T-C

71773497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60182729-G-A

71773497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60182729-G-T

71773508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60182706-G-A

71773508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30085
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60182706-G-T