20719754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137988245-T-C

20719786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137988225-C-T

20719811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137988203-G-T

20719869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137988149-G-T

20720007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137988010-T-C

20720040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987976-A-G

20720040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987976-A-T

20720085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987935-G-A

20720085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987935-G-C

http://identifiers.org/hco/1/GRCh38#20720241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137987836-C-A

20720241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987836-C-G

20720241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987836-C-T

20720267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987811-G-A

20720267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987811-G-T

20720367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987701-G-A

20720367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987701-G-T

20720369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987699-A-T

20720406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987650-T-C

20720451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987614-G-T

20720526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987393-G-A

20720526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987393-G-T

20720589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987306-G-T

http://identifiers.org/hco/1/GRCh38#20720691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137987207-C-A

http://identifiers.org/hco/1/GRCh38#20720731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137987171-C-A

20720731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987171-C-T

20720761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987143-G-A

http://identifiers.org/hco/1/GRCh38#20720787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137987130-A-C

20720856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987067-C-G

20720856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987067-C-T

20720899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987028-T-C

http://identifiers.org/hco/1/GRCh38#20720952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137987012-C-A

20720952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987012-C-T

http://identifiers.org/hco/1/GRCh38#20720957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137987007-C-A

20720957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137987007-C-T

20720976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986991-A-G

20721511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986829-G-A

20721511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986829-G-C

20721592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986760-G-A

20721592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986760-G-T

20721664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986685-G-T

20721685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986664-G-T

20721770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986575-T-A

20721770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137986575-T-C

20721859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137986499-C-T

20722042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986318-A-G

20722083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986279-T-A

20722084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986278-T-G

http://identifiers.org/hco/1/GRCh38#20722093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137986270-C-A

20722093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986270-C-G

20722093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986270-C-T

http://identifiers.org/hco/1/GRCh38#20722105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137986258-C-A

20722105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986258-C-T

20722112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986251-G-T

20722224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137986200-C-T

http://identifiers.org/hco/1/GRCh38#20722659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137985745-C-A

20722659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985745-C-T

20722730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985665-G-A

20722730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985665-G-C

20722730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985665-G-T

20722864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 137985529-C-T

20722865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137985528-A-G

20722865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137985528-A-T

20722918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137985475-A-G

20723339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985277-G-A

http://identifiers.org/hco/1/GRCh38#20723478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137985192-C-A

20723478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985192-C-T

20723485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985185-G-A

20723485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985185-G-T

20723522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985149-G-A

20723522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985149-G-C

20723522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985149-G-T

http://identifiers.org/hco/1/GRCh38#20723536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137985120-C-A

20723536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985120-C-T

20723552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985106-A-G

20723552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137985106-A-T

20723742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137984906-G-A

20723742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137984906-G-T

20723745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984903-C-T

20723772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984878-G-A

20723772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984878-G-T

http://identifiers.org/hco/1/GRCh38#20723782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137984868-A-C

20723782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984868-A-G

20723842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984799-T-C

http://identifiers.org/hco/1/GRCh38#20723861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137984784-C-A

20723903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984750-G-A

http://identifiers.org/hco/1/GRCh38#20723946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137984700-C-A

20723946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984700-C-T

20723956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984691-A-T

20724012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984633-T-C

http://identifiers.org/hco/1/GRCh38#20724052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137984613-C-A

20724052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984613-C-T

20724184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137984497-G-A

20724260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984415-C-T

20724282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984393-C-T

20724314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984361-A-G

20724322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984353-G-A

20724322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984353-G-C

20724322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137984353-G-T

20724341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137984327-A-T

20724484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137984182-T-G

20724518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137984139-T-G

http://identifiers.org/hco/1/GRCh38#20724610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137984047-C-A

20724610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137984047-C-G

20724610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137984047-C-T

20724653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983999-A-G

20724692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983966-A-G

20724692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983966-A-T

20724743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983921-C-G

20724743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983921-C-T

20724886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983779-A-G

20725167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983542-G-A

20725349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983424-C-T

20725502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983245-A-G

20725747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983090-T-G

http://identifiers.org/hco/1/GRCh38#20725835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137983041-C-A

20725841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983040-C-G

20725844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137983037-C-T

20726099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137982828-A-G

20726099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137982828-A-T

20726124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137982771-T-C

http://identifiers.org/hco/1/GRCh38#20726148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137982747-A-C

20726148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137982747-A-G

20726148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137982747-A-T

http://identifiers.org/hco/1/GRCh38#20726202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137982697-C-A

20726630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137982338-A-G

http://identifiers.org/hco/1/GRCh38#20726941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137982116-C-A

20727098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981983-G-A

20727098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981983-G-T

http://identifiers.org/hco/1/GRCh38#20727123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137981958-C-A

20727123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981958-C-T

http://identifiers.org/hco/1/GRCh38#20727135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137981946-C-A

20727135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981946-C-T

20727158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981924-G-A

20727158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981924-G-T

20727211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981871-G-T

20727321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981832-G-A

20727321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981832-G-C

20727350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981811-G-T

20727377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981787-T-A

20727377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981787-T-C

20727377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981787-T-G

20727416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981755-G-T

20727441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981735-G-A

20727441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981735-G-T

20727533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 137981652-C-T

20727708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981502-G-T

20727852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137981370-A-G

20727911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981310-T-A

20727911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981310-T-C

20727911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981310-T-G

http://identifiers.org/hco/1/GRCh38#20728025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137981200-C-A

20728025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981200-C-T

20728080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981146-G-A

20728080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981146-G-T

20728138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981070-G-A

20728138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981070-G-T

http://identifiers.org/hco/1/GRCh38#20728145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137981063-C-A

20728145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137981063-C-T

20728391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980830-T-A

20728452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980775-G-A

20728548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980561-G-C

20728584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980488-T-G

http://identifiers.org/hco/1/GRCh38#20728670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137980418-C-A

20728670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980418-C-T

20728678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980410-G-A

20728830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980285-C-T

20728877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980245-T-C

20729003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137980123-G-A

20729403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137979835-C-G

http://identifiers.org/hco/1/GRCh38#20729424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137979814-C-A

20729857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137979433-A-G

http://identifiers.org/hco/1/GRCh38#20729900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137979389-C-A

20729962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137979337-C-T

20730268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137979088-T-G

20730386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137979006-G-A

20730579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137978848-C-T

http://identifiers.org/hco/1/GRCh38#20730675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137978796-C-A

http://identifiers.org/hco/1/GRCh38#20730720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137978771-C-A

20730720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137978771-C-T

20730766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978732-A-T

20730786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978708-G-A

20730786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978708-G-T

20730848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978665-G-T

http://identifiers.org/hco/1/GRCh38#20731086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137978449-C-A

20731086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978449-C-G

20731086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978449-C-T

http://identifiers.org/hco/1/GRCh38#20731096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137978439-C-A

20731096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978439-C-T

20731602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137978056-A-G

http://identifiers.org/hco/1/GRCh38#20732051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137977778-C-A

20732075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137977754-T-C

20732242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137977585-C-T

http://identifiers.org/hco/1/GRCh38#20732244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137977583-C-A

20732365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137977519-C-T

http://identifiers.org/hco/1/GRCh38#20732389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137977494-C-A

20732389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137977494-C-T

20732407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137977478-T-C

20732407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137977478-T-G

20732545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137977402-G-T

20732560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137977383-A-G

http://identifiers.org/hco/1/GRCh38#20732712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137977291-C-A

20732712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137977291-C-T

20732773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137977242-G-A

20732773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137977242-G-T