126867761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56904710-T-C

http://identifiers.org/hco/5/GRCh38#126867762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56904711-C-A

126867762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56904711-C-T

http://identifiers.org/hco/5/GRCh38#126867824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56904756-C-A

126867824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56904756-C-T

126867832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56904765-C-T

126867911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56904856-G-T

126868067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56906350-T-A

126868067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56906350-T-C

126868329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56906830-G-A

http://identifiers.org/hco/5/GRCh38#126868347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56906855-C-A

126868347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56906855-C-T

126868407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56906883-T-C

126868464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56906933-C-T

126868557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907020-T-C

126868557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907020-T-G

126868576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907023-A-G

126868576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907023-A-T

126868587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907034-G-T

126868663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907091-A-G

126868734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907162-A-G

126868766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907194-A-G

http://identifiers.org/hco/5/GRCh38#126868894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56907321-C-A

126868894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907321-C-T

126868926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907353-C-T

126868944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907371-T-C

126868978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907405-T-C

126869038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907465-G-A

126869038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907465-G-T

126869107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907534-T-C

126869110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907537-A-G

126869112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907539-A-G

126869241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907660-G-A

126869284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907697-G-T

126869306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907715-G-A

126869306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907715-G-T

126869432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907845-G-A

126869496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907909-T-C

126869505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907918-G-A

126869505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56907918-G-T

126869698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56908093-G-A

126869843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56908210-T-C

126869993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3 prime UTR variant
orthologous variants: 56908353-G-A

126870241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56908614-G-A

126870241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56908614-G-T

126870255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56908628-T-C

126870478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56908871-G-T

126870663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56909052-G-T

http://identifiers.org/hco/5/GRCh38#126870933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56909297-C-A

126871226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56909552-A-G

126871544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56909715-C-T

126871607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56909781-T-C

126871612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56909786-T-A

126871643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56909813-A-G

126872681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56910592-C-G

126872842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56910746-T-C

126872843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56910747-G-C

126872931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56910828-G-A

126873135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911002-T-C

126873261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911119-G-A

126873362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911185-T-A

126873362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911185-T-C

126873593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911358-C-G

126873593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911358-C-T

126873705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911474-T-C

126873894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911656-A-G

126874094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911847-C-G

126874097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911850-T-C

126874178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911937-G-A

126874203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911961-G-A

126874203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56911961-G-T

126874458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912239-T-C

http://identifiers.org/hco/5/GRCh38#126874750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56912506-A-C

126874750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912506-A-T

126874861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56912591-G-A

126875333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56913137-C-T

126875586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56913381-C-T

126875832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56913628-C-T

126876068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56913878-T-G

126876072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56913885-G-A

126876121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56913934-C-T

126876170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56913976-T-C

126876196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56913992-C-T

126876331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56914119-A-G

126877089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915036-T-C

126877409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915328-C-T

126877438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915359-G-A

126877464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915383-G-A

126877573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915477-C-T

126877724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915635-C-T

126877906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915801-G-A

126877915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915810-C-T

126877916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915811-G-A

126878062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56915974-G-A

126878138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916045-G-T

126878141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916048-G-A

126878141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916048-G-C

126878141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916048-G-T

126878172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56916078-G-A

126878281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56916187-G-A

http://identifiers.org/hco/5/GRCh38#126878424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56916326-A-C

126878436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56916337-T-C

126878436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56916337-T-G

126878545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56916443-G-T

126878982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56917436-G-A

126879085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56917530-C-T

126879321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56917866-G-A

126880557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56919022-A-G

126880649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56919114-C-T

126880673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56919140-G-A

http://identifiers.org/hco/5/GRCh38#126880739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56919208-C-A

126880739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56919208-C-T

http://identifiers.org/hco/5/GRCh38#126880830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56919292-A-C

126880830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56919292-A-G

126881040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56919648-T-A

126881099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56920157-T-C

126881324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56920358-T-A

126881324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56920358-T-C

126881350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56920367-G-A

126881477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56920457-A-T

126881952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56920993-C-T

126882277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56921296-T-C

126882297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56921338-T-C

http://identifiers.org/hco/5/GRCh38#126882483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56921522-A-C

126882528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56921566-T-G

126882531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56921569-T-A

126882531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56921569-T-C

126882900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56921864-T-G

126882992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56921961-C-T

126883258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56922197-G-A

126883451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56922509-A-T

http://identifiers.org/hco/5/GRCh38#126883471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56922529-A-C

126883471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56922529-A-G

126883475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56922533-G-C

126883781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56923153-C-T

126883854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56923226-G-A

126883856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56923228-T-C

126884307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, undefined
orthologous variants: 56923645-G-T

126884351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, undefined
orthologous variants: 56923690-T-C

126884692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56923987-T-C

126884977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56924255-C-T

126885038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56924321-T-C

http://identifiers.org/hco/5/GRCh38#126885567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56926143-A-C

126885941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56926524-C-T

126887269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56927843-T-C

126887270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56927844-C-T

126887883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928358-C-G

126887940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928416-T-C

126888150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928614-A-G

126888155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928628-C-G

126888155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928628-C-T

http://identifiers.org/hco/5/GRCh38#126889743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56928727-C-A

126889785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928769-G-A

126889791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928774-G-A

126889810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928793-C-T

126889826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928809-T-C

126889834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928817-T-C

126889875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928857-C-T

126889913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928894-G-A

126889915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928896-T-C

126889918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928899-C-T

126889943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56928923-C-T

126890175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56929109-T-A

126890201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56929130-A-G

126897411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56930175-T-C

126897601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56930347-C-G

126897606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56930352-T-C

126898089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56930737-G-A

126898284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56930936-G-C

126898295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56930947-A-G

126898724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56931264-G-A

126898724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56931264-G-T

http://identifiers.org/hco/5/GRCh38#126898775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56931313-A-C

126898800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56931337-T-C

126898816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56931353-C-G

126898841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron variant
orthologous variants: 56931378-T-G

126898922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56931461-C-T

126899086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56931638-T-A

http://identifiers.org/hco/5/GRCh38#126899213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56931756-A-C

126899214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56931757-A-G

126899222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56931772-G-T

126899250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56931800-C-T

126899283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56931832-G-A

126899283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56931832-G-C

126899283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56931832-G-T

126899348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56931896-G-A

126899348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56931896-G-T

126899519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932072-A-G

126899882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932913-T-C

126899885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932916-T-C

126899946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56932979-T-C

126899973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933007-C-T

126900076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933121-C-G

126900076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933121-C-T

126900136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933182-A-T

126900349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933421-G-T

126900352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933424-T-C

126900398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933470-C-T

126900534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933604-G-A

126900536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933606-C-T

126901019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933769-C-T

126901087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56933813-C-G

http://identifiers.org/hco/5/GRCh38#126901884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56934491-A-C

126901903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934510-C-G

http://identifiers.org/hco/5/GRCh38#126902019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56934626-A-C

126902160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934746-C-T

126902317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56934907-G-A

126902971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935551-G-C

126902986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935565-A-G

126903118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935605-T-C

126903148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935631-T-G

126903288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935733-G-A

126903306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935751-T-C

126903321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935766-T-C

126903339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935790-A-T

http://identifiers.org/hco/5/GRCh38#126903409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56935860-C-A

126903409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56935860-C-T

126910009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56936864-T-C

126910009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56936864-T-G

126910018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56936873-C-T

126910084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56936939-C-G

126910279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56937119-G-T

126911858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56937930-C-T

126911885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56937954-T-C

http://identifiers.org/hco/5/GRCh38#126911929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56937991-C-A

126911988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56938048-T-C

126912146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56938211-C-T

126912485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938545-A-G

126912523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938584-T-A

126912612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938669-A-T

126912688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938746-G-A

126912923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56938982-G-A

126912967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56939026-C-T

126913123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56939170-G-C

126913448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56939452-T-G

126913539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56939542-G-A

126913702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56939692-T-C

126913789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56939761-T-C

126914510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940334-T-C

126914612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940429-T-C

126914634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940451-A-G

126914637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940454-G-T

126914657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940474-G-C

126914657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940474-G-T

126914728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56940568-C-T

http://identifiers.org/hco/5/GRCh38#126914837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56940644-A-C

126914853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56940660-G-T

126914880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56940686-A-G

126914893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56940699-T-C

126915065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56940871-T-C

126915143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940949-G-A

126915174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56940980-G-C

http://identifiers.org/hco/5/GRCh38#126915219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56941024-C-A

126915219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56941024-C-G

126915219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56941024-C-T

http://identifiers.org/hco/5/GRCh38#126915722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56942600-C-A

126915722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56942600-C-T

126915756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56942634-G-A

126915798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56942678-C-G

126916367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943178-C-T

126916584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943379-T-C

126916675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943538-T-A

126916688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943556-G-C

126916692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943560-G-C

126916702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943570-C-G

126916734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943602-G-C

126916843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56943716-C-T

126917276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944090-T-C

126917621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944492-G-A

126917691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944564-A-G

126917697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944577-T-C

http://identifiers.org/hco/5/GRCh38#126917717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56944612-C-A

126917717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944612-C-T

126917829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944720-A-G

http://identifiers.org/hco/5/GRCh38#126917835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56944726-A-C

126917835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944726-A-G

126917835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944726-A-T

126917854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944745-T-C

126917854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944745-T-G

126917859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944750-T-A

126917859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944750-T-C

http://identifiers.org/hco/5/GRCh38#126917867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56944788-C-A

126917867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944788-C-G

126917867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56944788-C-T

126918085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56945005-A-G

126918395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56945327-C-T

126918449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56945385-T-C

126918452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56945388-C-T

126918746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945682-C-T

http://identifiers.org/hco/5/GRCh38#126918893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56945822-A-C

126918903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945832-T-A

126919023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56945960-T-C

126919356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946043-C-G

126919356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946043-C-T

126919551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946220-C-T

126919674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56946337-T-G

126919704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56946358-C-T

126919897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946529-C-T

126919914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946547-G-A

126919926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946559-G-A

126919944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946576-A-G

126920130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56946896-C-T

http://identifiers.org/hco/5/GRCh38#126920152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56947001-A-C

126920369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947209-A-G

126920633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947466-G-A

126920760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947547-A-T

126920995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947755-C-T

126921029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56947790-A-T

http://identifiers.org/hco/5/GRCh38#126921062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56948055-A-C

126921276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948267-G-T

126921377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948368-G-C

126921494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948480-T-C

126921680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948649-T-C

126921732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948706-T-C

126921892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56948864-A-G

126922091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949064-A-G

126922128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949103-G-A

126922128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949103-G-C

126922227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949239-T-C

126922269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949371-C-T

126922422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56949884-C-G

126923216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56950181-G-A

126923326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56950306-G-A

126923336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56950316-G-A

126923472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56950442-G-T

126923574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56950506-T-C

126923949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56951034-T-C

http://identifiers.org/hco/5/GRCh38#126924236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56951308-C-A

126924236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56951308-C-T

126924391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56951464-G-A

126924509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56951573-C-T

126924522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56951586-C-T

126924702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56951760-C-T

126924776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56951834-T-G

http://identifiers.org/hco/5/GRCh38#126925744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56952809-A-C

126927251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56953837-G-A

126927351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56953932-G-A

126927573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954115-C-T

126927582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954124-C-T

126927645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954163-C-T

126927703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954220-G-A

126927703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954220-G-T

126927732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954257-T-C

126927892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954420-T-C

126928213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954743-C-T

126928444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954954-T-C

126928468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56954984-G-A

http://identifiers.org/hco/5/GRCh38#126928484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56955009-A-C

126928484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56955009-A-T

126929053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56955744-A-T

126929316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56956106-G-C

126930462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56957189-C-G

126930492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56957221-T-C

126930698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56957351-G-A

126930733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56957379-G-A

126931343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56957929-G-A

126931413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56957996-G-A

126931522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56958095-C-T

http://identifiers.org/hco/5/GRCh38#126932263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56958881-C-A

126932263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56958881-C-G

126932355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56958935-C-T

126932559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959055-T-C

126932670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959155-C-T

126932789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959248-C-T

126932849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959306-T-C

126932909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959365-A-G

126933334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959718-G-A

126933352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959736-C-T

126933830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959901-G-A

126933903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56959975-G-A

126934035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56963345-T-A

126934044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56963354-A-G

126934322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56963594-G-A

126934433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56963696-T-C

126934436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56963699-T-C

126934483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56963756-C-T

126934638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56963896-T-G

126936237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56965207-G-A

126936512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56965474-G-A

126936567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56965531-T-C

126936858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56965819-A-G

126938078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56966990-A-G

http://identifiers.org/hco/5/GRCh38#126938658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56967397-C-A

126939149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56967861-T-C

http://identifiers.org/hco/5/GRCh38#126939436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56968125-C-A

126939904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56969309-G-A

126940143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56969543-C-T

126940152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56969557-T-C

126941150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56970016-A-G

http://identifiers.org/hco/5/GRCh38#126941365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56970221-C-A

126941629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56970475-T-C

126941841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56970701-G-T

126941995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56970860-T-A

126942214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56971082-G-T

126942370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56971228-C-T

126942741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56971618-T-C

126945093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56972548-G-A

126945127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56972576-G-A

126945212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56972654-T-C

126945256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56972698-A-G

126945447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56972890-G-C

126945480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56972925-G-T

126947380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56975292-C-G

126947383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56975295-G-C

126947396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56975308-A-G

126947405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56975312-C-T

126947406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56975313-T-C

126947622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56975549-C-T

http://identifiers.org/hco/5/GRCh38#126947708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56975608-A-C

126947708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56975608-A-G

126949047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976150-A-T

126949054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976157-C-T

126949211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976310-C-T

126949241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976340-C-T

126949366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976466-T-C

126949454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976553-C-T

126949467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976560-C-T

126949583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976687-C-T

126949606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976710-C-T

126949738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56976845-C-G

126949912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56977018-G-A

http://identifiers.org/hco/5/GRCh38#126950104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56977232-C-A

126950449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56977540-T-C

http://identifiers.org/hco/5/GRCh38#126950615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56977670-C-A

126950680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56977733-A-G

126950734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56977790-C-T

126951298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56978334-C-T

126951616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56978598-T-C

126951638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56978620-C-G

126951638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56978620-C-T

126951756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56978734-A-G

126951777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56978755-C-T

126952304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56978976-G-C

126952345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56979020-T-G

http://identifiers.org/hco/5/GRCh38#126952936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56979305-A-C

126953033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56979398-G-A

126953156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56979725-C-T

126955165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56983140-G-A

126955202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56983169-G-C

http://identifiers.org/hco/5/GRCh38#126955447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56983416-C-A

126955447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56983416-C-T

126955542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56983502-G-C

126955611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56983574-T-C

126955826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56983791-T-C

http://identifiers.org/hco/5/GRCh38#126955878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56983838-A-C

126956053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984008-T-A

126956053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984008-T-C

126956066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984021-G-A

126956194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984128-T-C

126956209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984143-G-A

126956209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984143-G-C

126956231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984163-C-T

126956835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984296-C-T

126957151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56984728-C-T

126957703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56985311-T-A

http://identifiers.org/hco/5/GRCh38#126957812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56985586-C-A

126958230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56985980-T-C

126958244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56985989-C-T

126958472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56986182-C-T

http://identifiers.org/hco/5/GRCh38#126958488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56986198-C-A

126959933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56989003-C-T

126960188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56989251-T-C

126960401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56989459-A-G

126960649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56989695-C-T

126961248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56990256-T-C

http://identifiers.org/hco/5/GRCh38#126961431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56990434-C-A

126961431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56990434-C-T

126961709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56990758-C-T

126961984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56991031-G-A

126962079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991121-T-A

http://identifiers.org/hco/5/GRCh38#126962202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56991257-C-A

126962885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991551-A-G

126963125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991767-T-C

126963305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991969-T-A

126964979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992495-G-A

126965137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992652-C-T

126965220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992735-A-T

126965372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992896-G-A

126965392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993058-T-C

126965468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993140-C-T

126965551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993222-T-C

126965574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993248-A-G

126965776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993422-G-A

126966248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993906-A-G

126966270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993926-C-G

126966270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993926-C-T

http://identifiers.org/hco/5/GRCh38#126966323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56993983-A-C

126966514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56994170-A-G

126966713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56994596-C-T

126966750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56994633-A-G

126966796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56994674-C-T

126966858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56994739-C-T

126967166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56994884-C-T

126967198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56994916-C-T

126967963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56995497-G-C

126967986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56995518-A-G

126967994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56995526-C-T

126968948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56996047-C-G

126969008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56996100-A-G

126969142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56996235-A-T

http://identifiers.org/hco/5/GRCh38#126970445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56997139-A-C

126970775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56997452-C-T

126970793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56997470-A-G

126971587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56999272-C-T

126971624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56999308-C-G

http://identifiers.org/hco/5/GRCh38#126972148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56999818-A-C

126972197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56999864-T-C

126972273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56999949-G-A

http://identifiers.org/hco/5/GRCh38#126972279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56999955-C-A

http://identifiers.org/hco/5/GRCh38#126972285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#56999961-A-C

126972310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56999979-T-C

126972390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57000054-C-T

126972408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57000067-C-G

126972656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57000313-A-G

126972731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57000382-T-C

126972908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57000918-A-G

126973005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001044-C-T

126973018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001057-C-T

126973077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001121-T-C

126973230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001298-C-T

126973316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001382-C-G

126973323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001391-G-C

126973366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001434-C-T

126973466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001519-G-A

126973466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001519-G-T

126974713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002511-G-A

126974727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002525-C-T

126974863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002671-A-G

126974936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002743-G-T

126975675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002946-A-G

126975741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003006-G-A

126975884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003135-G-A

126975927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003172-G-A

126976535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003663-G-C

http://identifiers.org/hco/5/GRCh38#126976634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57003759-C-A

126976732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003858-T-C

126976958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004073-G-A

126977002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004117-G-A

126977110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004228-T-C

126977295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004351-T-A

126977319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004380-T-A

126977360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004421-T-C

126977567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004610-C-T

126977615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004655-C-T

126977674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004714-T-C

126978304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005357-G-A

126978420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005483-A-T

126978655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005712-A-T

126978718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005773-C-G

126978808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005855-G-A

126979062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57006069-T-G

126979088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57006096-T-C

126979154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57006190-C-T

http://identifiers.org/hco/5/GRCh38#126979249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57006562-C-A

126979481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57006823-T-C

126979525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57006875-T-C

126979668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007068-G-T

126979670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007070-C-T

126980121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007434-A-T

http://identifiers.org/hco/5/GRCh38#126980123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57007436-C-A

126980169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007480-T-C

126980329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007646-G-C

126980726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007746-G-A

126981008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57008029-T-C

126981257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57008633-T-C

126981263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57008639-C-T

126981462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57008830-C-G

126981693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009059-T-C

126981850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009223-T-C

126981850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009223-T-G

126981935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009323-T-G

126981940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009327-A-T

126982015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009401-T-C

http://identifiers.org/hco/5/GRCh38#126982528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57011002-A-C

126983167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011843-G-A

126983347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012027-G-A

126983440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012123-A-G

126983440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012123-A-T

126983531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012216-C-G

126983676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012359-C-T

126983739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012425-G-A

http://identifiers.org/hco/5/GRCh38#126983957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57012634-A-C

http://identifiers.org/hco/5/GRCh38#126984063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57012735-C-A

126984077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012745-C-T

126984078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012746-G-A

126984108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012773-T-C

126984187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012853-T-C

126984526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013181-G-C

126984616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013268-C-G

126984683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013329-T-C

http://identifiers.org/hco/5/GRCh38#126984881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57013518-A-C

126984945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013582-G-A

126984994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013630-G-C

126985107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013736-A-T

126985860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57014344-G-A

126986127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57014602-C-G

126986127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57014602-C-T

http://identifiers.org/hco/5/GRCh38#126986217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57014680-C-A

126986219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57014682-G-A

126986336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57014795-G-A

http://identifiers.org/hco/5/GRCh38#126986639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57015099-A-C

126986639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57015099-A-G

126987049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57016477-G-C

126987177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57016583-T-A

126987177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57016583-T-C

126987258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57016665-C-T

126987386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57016783-G-C

http://identifiers.org/hco/5/GRCh38#126987516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57016900-C-A

126987516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57016900-C-T

126987668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57017077-G-A

126987668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57017077-G-T

126987760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57017473-C-T

126987771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57017484-A-G

126987894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57017598-A-G

http://identifiers.org/hco/5/GRCh38#126987925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57017628-A-C

126988205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57017816-C-T

126988368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57017960-C-T

126988434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57018026-A-G

126989766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57020952-T-C

126992012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021262-T-C

126992403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021648-T-C

126992532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021780-T-C

126992684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021905-A-G

126992763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021976-G-A

126992763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021976-G-T

126993115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57022012-G-A

126993129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57022026-G-A

126993243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57022141-G-T

126993521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57022802-T-C

126993552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57022834-G-T

126993604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57022886-G-C

126993733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57023009-C-T

126993789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57023062-C-T

126995290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57024663-A-G

126995551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57024887-G-C

126995699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57025233-C-G

126995864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57025399-C-G

126995864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57025399-C-T

126995999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57025526-A-G

126996052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57025565-T-A

http://identifiers.org/hco/5/GRCh38#126996090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57025603-C-A

http://identifiers.org/hco/5/GRCh38#126996514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57025979-C-A

126996514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57025979-C-G

126996520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57025985-T-A

126996648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57026106-T-C

126996791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57026243-C-T

126996853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57026310-T-C

126996922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57026368-T-A

126996922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57026368-T-C

126996988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57026438-A-G

126997201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57027576-T-A

126997332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57027703-G-A

126997429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57027798-C-T

126997644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029128-T-C

126997763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029330-G-T

126997777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029344-C-T

126998729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029491-T-C

126998729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029491-T-G

126998890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029881-G-A

126999170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030147-T-C

126999267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030237-T-C

126999440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030397-C-T

126999641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030596-G-T

126999676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030636-T-C

127000087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030922-T-C

127000277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031092-G-A

127000619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031408-T-C

127000687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031493-T-C

127001507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57032178-G-A

127001514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57032185-G-A

127002132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57032786-C-G

http://identifiers.org/hco/5/GRCh38#127002142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#57032791-C-A

127002297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57032946-G-A

127002297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57032946-G-C

127002429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57033070-T-A

127002429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57033070-T-C

127002708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033332-C-G

127002734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033356-G-A

127002979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033609-G-C

127002979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033609-G-T

127003179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033820-C-T

127003740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033878-G-A

127003785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033933-T-A

127003992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034117-C-T

127004058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034385-C-T

127004378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034734-A-G

127004383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034747-A-T

127005638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57035707-T-G

127005642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57035711-T-C

127005682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57035751-C-T

http://identifiers.org/hco/5/GRCh38#127006234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57036719-C-A

127006239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57036724-A-G

127006424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57036917-C-G

127006425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57036918-C-T

http://identifiers.org/hco/5/GRCh38#127006437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57036930-C-A

127006529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037022-T-C

127006987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037453-C-G

127007040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037494-C-T

127007044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037498-G-A

127007107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037561-A-G

127007168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037617-T-C

127007211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037657-C-T

http://identifiers.org/hco/5/GRCh38#127007250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57037695-A-C

127007631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57038364-G-C

127007971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57038837-T-C

127008080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57038922-A-G

127008284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039388-G-T

127008404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039509-T-C

http://identifiers.org/hco/5/GRCh38#127008422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57039526-A-C

127008437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039555-T-C

http://identifiers.org/hco/5/GRCh38#127008443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57039561-C-A

127008477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039598-A-G

127008479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039600-T-C

127008481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039602-T-C

127008594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039714-C-G

127008988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039988-G-C

127009103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040103-A-G

127009155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040127-G-T

127009283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040258-G-A

127009413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040372-G-A

127009444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040399-T-C

127009486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040447-T-C

127009874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040805-C-T

http://identifiers.org/hco/5/GRCh38#127009903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57040834-C-A

127010230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041161-G-T

http://identifiers.org/hco/5/GRCh38#127010604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57041541-A-C

127010631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041568-A-G

127010761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041689-A-G

127011253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57042253-C-T

127011352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57042337-C-G

127011352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57042337-C-T

127011402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57042387-T-C

127011542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57042536-T-A

127011542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57042536-T-C

127011643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57042637-C-T

127012056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57043053-T-C

127012425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57043414-T-G

127012480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57043462-G-T

127012498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57043480-T-C

127012598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57043570-T-G

127012614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57043580-G-A

127012810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57043776-C-T

127012929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57043882-A-G

http://identifiers.org/hco/5/GRCh38#127013502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57044457-C-A

127013502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57044457-C-T

127015289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57045508-T-C

127018363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57046437-T-G

127018629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57046680-T-C

127018774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57046826-T-C

127019204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57047264-G-T

http://identifiers.org/hco/5/GRCh38#127019230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57047295-C-A

127019230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57047295-C-T

127019320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57047395-T-C

127019329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57047403-C-G

127020172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57048053-A-G

127020214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57048094-A-G

127020927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049365-C-G

127020927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049365-C-T

127021050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049479-C-T

127021134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049569-C-T

127021237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049645-A-G

127021464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049865-C-T

127021493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049898-G-A

127021585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049939-C-T

127021586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049940-G-A

127021595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049949-T-C

127021640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049993-C-T

127022148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050224-G-A

127022163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050239-T-A

127022245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050319-T-C

127022326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050399-G-A

127022370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050440-G-C

127022534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050964-A-G

127022557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050985-A-G

127022601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57051044-G-A

http://identifiers.org/hco/5/GRCh38#127022615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57051058-C-A

127022909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57051332-G-A

127023015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57051439-C-T

127024015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57051805-G-T

127024044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57051833-T-C

127024086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57052003-T-C

127024192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57052104-G-C

127025568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57053837-A-G

127025955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57054175-A-G

127026093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57054310-T-A

127026093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57054310-T-C

127026094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57054311-A-T

127026480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57054849-A-G

127026593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57054953-G-T

127027164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57055512-G-A

127027164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57055512-G-C

127027291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57055589-G-C

127027494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57055765-A-G

127027605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57055858-G-A

127027606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57055859-G-A

127028248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57056415-C-T

127028550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57056723-C-T

127028605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57056769-T-C

127028762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57056909-T-C

127029006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57057154-G-A

http://identifiers.org/hco/5/GRCh38#127029080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57057229-C-A

127029080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57057229-C-T

127029155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57057304-G-A

127029155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57057304-G-C

127029374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57057485-C-T

http://identifiers.org/hco/5/GRCh38#127029639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57057743-C-A

127029782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57057859-G-T

127029974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57058031-G-A

127030144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57058189-C-T

127030377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5 prime UTR variant
orthologous variants: 57058406-C-T

http://identifiers.org/hco/5/GRCh38#127030419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57058449-C-A

127030419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5 prime UTR variant
orthologous variants: 57058449-C-T

127030430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5 prime UTR variant
orthologous variants: 57058460-C-T

127030447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5 prime UTR variant
orthologous variants: 57058477-G-T

127030525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28728
most severe consequence: 5 prime UTR variant
orthologous variants: 57058554-G-T