http://identifiers.org/hco/1/GRCh38#40300540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120912506-C-A

40300546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3 prime UTR variant
orthologous variants: 120912500-A-G

40300574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3 prime UTR variant
orthologous variants: 120912472-G-A

40300574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3 prime UTR variant
orthologous variants: 120912472-G-T

40300610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3 prime UTR variant
orthologous variants: 120912450-G-A

40300610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3 prime UTR variant
orthologous variants: 120912450-G-T

http://identifiers.org/hco/1/GRCh38#40300684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120912382-C-A

40300684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912382-C-T

http://identifiers.org/hco/1/GRCh38#40300690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120912376-C-A

40300691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912375-A-G

40300691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912375-A-T

40300697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912369-G-A

40300697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912369-G-T

http://identifiers.org/hco/1/GRCh38#40300703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120912363-C-A

40300703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912363-C-G

40300703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912363-C-T

40300707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912360-A-G

http://identifiers.org/hco/1/GRCh38#40300709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120912358-C-A

40300709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912358-C-T

40300711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912356-G-A

40300711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912356-G-C

40300722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912339-G-A

40300765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912296-G-T

40300849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912279-G-C

40300865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912262-G-A

40300865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120912262-G-T

http://identifiers.org/hco/1/GRCh38#40301025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120912131-C-A

40301186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120911986-G-A

40301366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120911806-G-A

40301467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911727-G-T

40301471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911723-A-G

http://identifiers.org/hco/1/GRCh38#40301505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120911691-C-A

40301505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911691-C-T

40301525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911681-T-A

40301551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911659-A-G

40301688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911634-A-G

40301744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911596-C-T

40301747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911593-T-C

40301768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911572-C-T

40301777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911563-G-T

40301782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911559-C-T

40301838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120911499-C-T

http://identifiers.org/hco/1/GRCh38#40301848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120911489-C-A

40301848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120911489-C-T

40301881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120911456-C-T

40301926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911414-T-G

http://identifiers.org/hco/1/GRCh38#40301943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120911399-C-A

40301969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911373-G-T

40302001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911352-A-T

40302002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911351-G-C

40302002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911351-G-T

40302023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120911330-C-T

http://identifiers.org/hco/1/GRCh38#40302767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120911007-A-C

40302767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120911007-A-G

40302907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910902-T-C

http://identifiers.org/hco/1/GRCh38#40302982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910832-C-A

40302982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910832-C-T

http://identifiers.org/hco/1/GRCh38#40302990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910824-C-A

40302990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910824-C-T

http://identifiers.org/hco/1/GRCh38#40302991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910823-A-C

40302991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910823-A-G

40303043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910770-G-T

40303108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910715-G-T

40303175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120910644-G-A

40303175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120910644-G-T

http://identifiers.org/hco/1/GRCh38#40303193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910626-C-A

40303193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120910626-C-G

40303438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910489-G-A

40303438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910489-G-C

40303438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910489-G-T

http://identifiers.org/hco/1/GRCh38#40303452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910475-C-A

40303452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910475-C-G

40303469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910459-A-G

http://identifiers.org/hco/1/GRCh38#40303471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910457-C-A

40303471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910457-C-T

40303543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120910386-C-T

http://identifiers.org/hco/1/GRCh38#40303561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910368-A-C

40303584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120910345-T-C

http://identifiers.org/hco/1/GRCh38#40303627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910302-C-A

40303628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120910301-C-T

http://identifiers.org/hco/1/GRCh38#40303629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910300-C-A

40303629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120910300-C-T

40303678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 120910251-T-C

40303726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910213-T-A

40303726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910213-T-G

40303731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910208-G-A

40303731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910208-G-T

http://identifiers.org/hco/1/GRCh38#40303734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910205-A-C

40303734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910205-A-G

40303734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910205-A-T

40303741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910193-G-A

40303741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910193-G-T

40303747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910187-G-A

40303747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910187-G-T

40303753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910181-G-A

40303753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910181-G-T

40303758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910175-G-A

40303758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910175-G-C

40303758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910175-G-T

40303785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910140-A-G

http://identifiers.org/hco/1/GRCh38#40303847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910078-C-A

40303847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120910078-C-T

40303872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910054-G-A

40303872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910054-G-C

http://identifiers.org/hco/1/GRCh38#40303894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910034-C-A

http://identifiers.org/hco/1/GRCh38#40303905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910022-C-A

http://identifiers.org/hco/1/GRCh38#40303906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120910021-C-A

40303906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910021-C-T

40303915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120910005-G-A

40303922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909998-G-A

40303922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909998-G-T

http://identifiers.org/hco/1/GRCh38#40303962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120909958-C-A

40303962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120909958-C-T

40303978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120909940-G-A

40303978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120909940-G-C

40303978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120909940-G-T

40304037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909867-G-A

40304037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909867-G-T

40304124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909754-T-A

40304124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909754-T-G

40304400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909544-A-G

40304525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120909426-T-C

40304646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909311-G-T

40304652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909305-T-C

40304710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909273-G-A

40304710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909273-G-C

40304710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909273-G-T

http://identifiers.org/hco/1/GRCh38#40304912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120909102-C-A

40304912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120909102-C-T

40305647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908993-G-T

40305666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908974-G-C

40305674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908966-C-T

40305889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908702-T-C

40305998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908603-G-T

40306017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908587-G-A

40306017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908587-G-C

40306017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908587-G-T

http://identifiers.org/hco/1/GRCh38#40306030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120908574-A-C

40306030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908574-A-G

40306059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908540-G-T

40306060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908539-A-G

40306060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908539-A-T

40306123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908473-C-G

40306127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908469-C-T

40306287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120908311-T-G

40306394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120908205-C-T

40306406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120908194-G-A

40306475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908159-A-T

http://identifiers.org/hco/1/GRCh38#40306528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120908105-C-A

40306532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908101-C-G

40306532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908101-C-T

40306747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120908036-C-T

http://identifiers.org/hco/1/GRCh38#40307308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120907795-C-A

40307308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907795-C-G

40307308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907795-C-T

40307322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907781-G-C

http://identifiers.org/hco/1/GRCh38#40307342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120907761-A-C

http://identifiers.org/hco/1/GRCh38#40307410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120907639-C-A

40307410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907639-C-T

40307584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907466-G-C

40307602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907450-A-G

40307637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907413-G-A

40307637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907413-G-T

40307680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907348-C-T

40307681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907347-C-G

40307716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120907311-G-A

40307835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907208-G-A

40307864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907181-C-T

40308046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907027-A-G

40308047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907026-G-A

40308047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120907026-G-T

40308082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120906996-C-T

40308178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120906924-C-G

40308301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120906802-G-A

40308301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120906802-G-C

40308351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120906759-C-T

40309435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903843-A-G

40309494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903771-G-A

40310015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903405-T-C

40310015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903405-T-G

40310046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903374-C-T

http://identifiers.org/hco/1/GRCh38#40310221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120903208-C-A

40310336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903089-G-A

40310336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903089-G-T

40310378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903046-C-G

40310378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903046-C-T

http://identifiers.org/hco/1/GRCh38#40310405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120903025-C-A

40310418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903012-G-A

40310418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903012-G-T

40310428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120903003-T-C

40310468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902963-G-A

http://identifiers.org/hco/1/GRCh38#40310584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120902853-C-A

http://identifiers.org/hco/1/GRCh38#40310600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120902838-C-A

40310662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902778-A-G

40310662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902778-A-T

40310788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902659-G-T

40310789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902658-T-C

http://identifiers.org/hco/1/GRCh38#40310790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120902657-C-A

40310790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902657-C-G

40310790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902657-C-T

40310801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902646-G-A

40310801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902646-G-T

40310870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902592-G-A

40310870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902592-G-T

40310895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902567-T-C

40310958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902531-C-T

40310965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902524-C-G

40310975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902513-G-A

40310975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902513-G-T

40310994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902493-G-T

http://identifiers.org/hco/1/GRCh38#40311406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120902113-A-C

40311406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902113-A-G

http://identifiers.org/hco/1/GRCh38#40311484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120902081-A-C

40311562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120902000-G-A

40311640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901936-T-C

40311675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120901900-G-A

40311675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120901900-G-C

40311751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901815-C-G

40311756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901810-C-T

40311766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901800-T-A

40311766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901800-T-C

40311798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901773-G-A

40311798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901773-G-T

40311802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901769-T-C

40311804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901767-T-C

40311806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901765-C-T

http://identifiers.org/hco/1/GRCh38#40311810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120901761-C-A

40311810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901761-C-T

http://identifiers.org/hco/1/GRCh38#40311843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120901728-C-A

40311844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901727-T-C

http://identifiers.org/hco/1/GRCh38#40311866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120901709-A-C

40311866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901709-A-G

40312019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901562-G-T

40312026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901555-G-A

40312040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901542-G-T

40312049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901533-T-A

40312049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901533-T-C

40312090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120901492-A-G

40312135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901446-T-C

40312138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901443-G-C

40312138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901443-G-T

40312152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901429-G-A

40312152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901429-G-T

40312197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901395-G-A

40312197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901395-G-T

40312224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901377-T-C

40312226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901375-T-A

40312238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901363-G-A

40312238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901363-G-C

40312238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901363-G-T

http://identifiers.org/hco/1/GRCh38#40312274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120901327-A-C

40312280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901321-G-C

40312303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901316-G-T

40312351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901290-C-G

40312351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120901290-C-T

40312427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120901237-G-C

40312427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120901237-G-T

40312480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 120901189-C-G

40312480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 120901189-C-T

40312484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120901185-A-G

40312537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901131-C-G

40312537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901131-C-T

http://identifiers.org/hco/1/GRCh38#40312620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120901046-A-C

40312648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120901017-C-T

http://identifiers.org/hco/1/GRCh38#40312668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900997-C-A

40312701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120900962-C-T

http://identifiers.org/hco/1/GRCh38#40312726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900949-C-A

http://identifiers.org/hco/1/GRCh38#40312749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900926-C-A

40312749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120900926-C-G

40312750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120900925-A-G

40312802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900873-T-C

40312806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900869-G-A

40312806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900869-G-T

http://identifiers.org/hco/1/GRCh38#40312810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900865-C-A

40312810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900865-C-T

http://identifiers.org/hco/1/GRCh38#40312820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900855-C-A

40312820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120900855-C-T

http://identifiers.org/hco/1/GRCh38#40312824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900851-C-A

40312824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120900851-C-T

40312848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900828-G-A

40312848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900828-G-T

http://identifiers.org/hco/1/GRCh38#40312897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900797-C-A

40312897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900797-C-G

40312897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900797-C-T

http://identifiers.org/hco/1/GRCh38#40312929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120900768-C-A

40313283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900623-C-T

40313336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120900563-T-G

40313435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900447-C-T

40313542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900339-T-C

40313597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120900269-C-T

40313974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120899876-C-T

http://identifiers.org/hco/1/GRCh38#40314103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120899744-C-A

40314103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120899744-C-T

40314319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120899559-A-G

40314350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 120899526-A-G

40314350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 120899526-A-T

40314430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120899462-C-G

40314430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120899462-C-T

40314439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120899453-G-C

40314465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120899425-C-T

40314767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120898995-G-A

40314933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120898854-G-A

40315200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120898584-A-G

40315200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120898584-A-T

40315328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120898482-G-A

40315328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120898482-G-T

40315444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898366-T-A

40315444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898366-T-C

40315453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898357-G-A

40315453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898357-G-T

40315459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898351-G-A

40315459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898351-G-C

40315459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898351-G-T

40315549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898275-T-A

40315549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898275-T-C

http://identifiers.org/hco/1/GRCh38#40315551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120898273-C-A

40315551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120898273-C-T

40315553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120898271-G-A

40315553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120898271-G-C

40315553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120898271-G-T

40315556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120898268-T-A

40315556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120898268-T-C

40315600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120898224-T-C

http://identifiers.org/hco/1/GRCh38#40315624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120898200-C-A

40315624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120898200-C-T

40315736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120898094-G-A

40315845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120897974-A-G

40315880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120897939-G-A

40315880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120897939-G-T

40315894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120897925-G-T

http://identifiers.org/hco/1/GRCh38#40315945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897877-C-A

40315945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120897877-C-T

http://identifiers.org/hco/1/GRCh38#40316014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897809-C-A

40316014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120897809-C-T

http://identifiers.org/hco/1/GRCh38#40316016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897807-C-A

40316016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120897807-C-T

http://identifiers.org/hco/1/GRCh38#40316054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897773-A-C

40316054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120897773-A-G

40316076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120897751-G-T

40316280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897613-G-A

40316582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897517-C-T

http://identifiers.org/hco/1/GRCh38#40316597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897502-C-A

40316599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897500-G-T

40316600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897499-G-T

40316629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897464-C-T

http://identifiers.org/hco/1/GRCh38#40316640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897453-C-A

40316640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897453-C-G

40316640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897453-C-T

40316644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120897442-G-A

40316644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120897442-G-T

http://identifiers.org/hco/1/GRCh38#40316679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897401-C-A

40316679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120897401-C-T

http://identifiers.org/hco/1/GRCh38#40316717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120897365-C-A

40316717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897365-C-T

40316769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120897313-G-A

40316769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120897313-G-T

40316898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120897184-C-G

40317051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897056-G-C

40317051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897056-G-T

40317097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897007-G-A

40317097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120897007-G-T

40317153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120896951-G-A

40317153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120896951-G-T

40317223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120896884-G-A

40317223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120896884-G-C

40317223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120896884-G-T

40317254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120896864-A-G

40317254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120896864-A-T

http://identifiers.org/hco/1/GRCh38#40317316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120896827-A-C

40317316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120896827-A-G

40317316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120896827-A-T

40317317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120896826-T-C

40317317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120896826-T-G

40317318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896825-G-C

40317318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896825-G-T

40317329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896808-G-A

40317329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896808-G-T

40317343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896795-T-A

40317343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896795-T-C

40317343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896795-T-G

http://identifiers.org/hco/1/GRCh38#40317413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120896746-C-A

40317413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896746-C-G

40317413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896746-C-T

40317414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896745-G-A

40317414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896745-G-T

40317427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896731-T-C

40317477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896656-A-G

http://identifiers.org/hco/1/GRCh38#40317548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120896584-C-A

40317548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120896584-C-T

40317618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: 120896508-G-A

http://identifiers.org/hco/1/GRCh38#40317708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120896435-C-A

40317708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: 120896435-C-T

http://identifiers.org/hco/1/GRCh38#40317726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120896417-C-A

40317726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: 120896417-C-G

http://identifiers.org/hco/1/GRCh38#40317742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120896399-C-A

40317742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: 120896399-C-T

40317798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2218
most severe consequence: non coding transcript exon variant
orthologous variants: 120896329-T-C