177728968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53713560-A-G

177729007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53713524-T-C

177729018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 53713513-G-A

177729018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 53713513-G-T

177729056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53713475-T-G

177729061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53713470-A-G

177729070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53713461-C-T

177729071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53713460-G-A

177729071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53713460-G-T

177729121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53713406-T-C

177729121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53713406-T-G

177729928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53712978-G-A

177729993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53712912-G-A

http://identifiers.org/hco/4/GRCh38#177730111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53712849-A-C

http://identifiers.org/hco/4/GRCh38#177736165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53704927-C-A

177736165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53704927-C-T

177736256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53704838-T-G

177737144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53704314-T-C

177737342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53704113-A-G

177737395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53704050-T-C

http://identifiers.org/hco/4/GRCh38#177737587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53703854-C-A

177737647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703801-A-G

177737717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703729-A-G

177737860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703586-T-C

177737862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703584-C-T

177737863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703583-G-A

177737864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703582-G-A

177737911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703524-T-C

http://identifiers.org/hco/4/GRCh38#177737980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53703451-C-A

177737980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53703451-C-T

177738776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53702562-T-C

177738839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53702484-T-G

177739487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53701623-C-T

177739637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53701475-G-A

177739637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53701475-G-T

177740369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53701262-G-A

177740440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53701191-G-T

177740508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53701125-G-A

177740553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53701080-A-G

177740870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53700447-T-C

177741055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53700257-C-T

177741263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53700048-T-C

177741295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53700013-A-G

177741343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53699845-A-G

177741644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53699582-A-G

177743849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53698000-A-G

177743878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53697971-C-T

177743880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53697969-T-C

http://identifiers.org/hco/4/GRCh38#177743947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53697897-A-C

http://identifiers.org/hco/4/GRCh38#177744040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53697814-A-C

177744056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53697798-T-G

177744120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53697743-T-C

177744185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53697685-G-C

177744185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53697685-G-T

177744441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53697434-G-A

177747789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53690452-A-G

177748067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53690196-A-G

177748070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53690193-G-A

177748455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689803-A-G

177748706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689549-A-G

177748721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689536-G-A

177748809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689450-A-G

177748824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689435-A-G

177748884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689376-G-A

177748884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689376-G-C

177748959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53689311-T-G

177754397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53688173-A-G

177754404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53688166-A-G

177754607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687966-A-G

177754611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687962-T-C

177754724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687848-T-A

177754746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687816-C-T

177754791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687764-G-A

177754878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687686-G-T

177754909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687606-A-T

177755011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687518-A-G

177755070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687455-T-C

177755257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687272-T-A

177755257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687272-T-C

177755286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687243-C-G

177755286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687243-C-T

177755356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687172-C-G

177755356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53687172-C-T

177755558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686974-T-C

http://identifiers.org/hco/4/GRCh38#177755571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53686962-A-C

177755574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686959-C-G

177755574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686959-C-T

177755584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686951-T-C

177755753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686786-T-C

177755818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686701-A-G

177755867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686654-G-A

177755867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686654-G-C

http://identifiers.org/hco/4/GRCh38#177755880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53686641-C-A

177755944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686570-C-G

177756169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686409-C-T

177756518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53686026-T-C

177757234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53685347-A-G

177758048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53684079-T-A

177758048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53684079-T-C

177758156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53683964-G-A

177758238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53683888-T-G

177758267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53683863-C-G

177760078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53679248-A-G

http://identifiers.org/hco/4/GRCh38#177760165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53679173-A-C

177760193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53679148-A-G

177760235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53679105-T-G

177760275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53679060-C-T

177760339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678998-A-G

177760575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678774-G-C

177760575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678774-G-T

177760955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678400-G-A

177761017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678344-G-A

177761042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678320-T-C

177761066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678296-A-T

177761079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678283-C-T

177761302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53678058-G-A

177761399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677973-G-A

177761409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677963-T-A

177761409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677963-T-C

177761441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677940-T-C

177761465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677918-A-T

http://identifiers.org/hco/4/GRCh38#177761509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53677871-C-A

177761524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677859-C-G

177761651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677772-G-A

177761651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677772-G-T

177761660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677763-C-G

177761691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677733-C-G

177761712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677724-C-T

177761753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677691-G-A

177761823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677623-T-C

177761845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677608-T-C

177761885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677568-T-C

177761901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677552-C-T

177761922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677541-T-C

177761927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677533-G-A

177761976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677487-G-C

177762366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53677205-C-T

177762592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53676998-A-G

177765257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53676413-T-C

177765496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53676188-A-T

177765596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53676091-T-C

177765673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53676018-A-G

177765896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53675837-A-G

177765920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53675820-T-C

177765955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53675782-C-T

177766191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53675533-G-A

177768816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674824-A-G

177768817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674823-T-C

http://identifiers.org/hco/4/GRCh38#177768951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53674729-A-C

177768951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674729-A-G

177769092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674596-A-G

177769123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674562-G-A

http://identifiers.org/hco/4/GRCh38#177769210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53674459-A-C

177769274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674392-C-T

177769400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674262-G-T

http://identifiers.org/hco/4/GRCh38#177769556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53674103-C-A

177769556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53674103-C-T

177770039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53673627-T-C

177770079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53673586-G-A

177770138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53673531-C-T

177770300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53673395-G-C

177770532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53673157-T-G

177770726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672960-C-G

177770762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672928-G-T

177770879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672829-T-C

177770909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672799-C-T

177771155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672649-A-T

177771303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672490-G-T

177771436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672340-G-T

177771489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53672292-A-G

http://identifiers.org/hco/4/GRCh38#177771522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53672260-C-A

177771758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671981-C-T

177771907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671833-G-T

177771987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671754-A-G

177772018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671723-G-A

177772018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671723-G-T

177772097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671543-C-T

177772133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671510-A-T

http://identifiers.org/hco/4/GRCh38#177772250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53671389-A-C

177772278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671363-T-C

177772298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671343-G-A

177772536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671087-A-G

177772651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53671005-T-G

177772773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53670896-G-A

177773424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53663116-A-G

177773436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53663104-G-A

177774626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659661-A-G

177774701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659594-A-G

177774718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659577-G-A

177774773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659533-A-G

177774950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659383-A-G

177774990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659340-T-C

177775017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659319-T-A

177775174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659166-A-G

http://identifiers.org/hco/4/GRCh38#177775208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53659132-C-A

177775329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53659028-A-G

177775382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53658954-T-C

177775486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53658851-T-C

177775807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53658018-A-G

177775888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53657939-G-T

177776413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53657556-G-A

177776436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53657523-T-C

177776488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53657472-G-T

177776571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 53657393-C-T

177776731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53657231-A-T

177778195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53655244-G-A

177778209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53655212-G-T

http://identifiers.org/hco/4/GRCh38#177778436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53655008-C-A

177779187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652963-A-G

177779244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652901-C-G

177779406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652778-A-T

177779414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652770-T-G

177779440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652741-T-C

177779484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652697-G-T

177779492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652689-C-T

177779519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652652-A-T

177779633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652546-T-C

177779708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53652459-A-T

http://identifiers.org/hco/4/GRCh38#177779909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53652251-A-C

http://identifiers.org/hco/4/GRCh38#177790230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53650786-A-C

177790293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53650738-T-C

177790305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53650726-A-G

177790590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53650469-G-A

177790822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53650268-A-T

177790855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53650237-T-A

177790909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53650183-T-G

177791109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53649982-T-C

177791287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53649495-C-T

177791573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53649272-A-G

177791610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53649234-A-G

177792704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53647122-G-C

177793041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53646770-T-G

177793077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53646733-A-G

177793245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53646544-G-A

177793345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53646438-A-G

177793476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53646301-A-T

http://identifiers.org/hco/4/GRCh38#177793544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53646184-C-A

http://identifiers.org/hco/4/GRCh38#177793578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53646123-C-A

177793578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53646123-C-T

177793807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53645835-G-A

177793853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53645788-A-G

177793995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53645639-A-G

http://identifiers.org/hco/4/GRCh38#177795364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53640769-C-A

177795602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53640571-T-C

177795675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53640441-G-A

177795685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53640431-G-A

177795711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53640409-A-G

http://identifiers.org/hco/4/GRCh38#177795789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53640347-C-A

177795834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53640302-A-G

177799664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53637661-T-A

177799717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53637608-C-G

177800300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53637055-A-G

177800361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53636999-A-G

177801644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53636814-C-T

177801844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53635099-A-G

177801918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53635026-A-G

177802199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53634759-G-A

177802223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53634735-C-T

177802380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53634580-G-C

http://identifiers.org/hco/4/GRCh38#177802473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53634483-C-A

177802490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53634466-T-G

177802547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53634408-T-C

177802681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53634276-C-T

http://identifiers.org/hco/4/GRCh38#177802778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53634179-A-C

177802946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53634012-A-G

http://identifiers.org/hco/4/GRCh38#177802962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53633997-C-A

177803282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53633429-T-A

177803353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53633381-T-G

177803453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53633282-G-A

177803453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53633282-G-T

http://identifiers.org/hco/4/GRCh38#177803533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53631959-A-C

177803685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53631806-A-T

177803697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53631796-A-G

177804102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53631378-G-T

177804243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53631244-C-T

http://identifiers.org/hco/4/GRCh38#177804255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53631231-C-A

177804255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53631231-C-T

177804546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630946-A-G

177804546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630946-A-T

177804636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630853-A-G

177804646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630844-G-A

177804704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630786-T-A

177804722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53630761-A-G

177809295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53625650-T-A

177809307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53625640-A-G

177809466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53625484-T-A

177809782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53625173-G-A

177809785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53625138-T-A

177809809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53625114-T-G

http://identifiers.org/hco/4/GRCh38#177809892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53625002-A-C

177809979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624915-G-T

177810194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624704-G-C

177810399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624498-A-G

177810508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624349-C-T

177810531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624331-G-A

177810545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53624319-T-C

177811549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53623826-C-G

177811549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53623826-C-T

177811671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53623688-A-G

177811771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53623602-T-C

177811802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53623571-T-C

177811865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53623511-T-A

http://identifiers.org/hco/4/GRCh38#177811890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53623486-A-C

177811961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53623414-G-T

177812384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53623253-T-A

http://identifiers.org/hco/4/GRCh38#177812459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53623183-C-A

http://identifiers.org/hco/4/GRCh38#177812542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53623122-C-A

177812542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53623122-C-T

http://identifiers.org/hco/4/GRCh38#177812548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53623116-C-A

177812548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53623116-C-T

177812557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53623107-G-T

177812592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53623064-A-G

177812604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53623052-T-C

http://identifiers.org/hco/4/GRCh38#177812700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53622957-C-A

177812700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622957-C-G

177812700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622957-C-T

177812718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622939-G-A

177812718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622939-G-C

177812718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622939-G-T

177812740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622918-A-G

177812768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622904-T-C

177812784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622889-T-C

177812805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622867-A-G

http://identifiers.org/hco/4/GRCh38#177812898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53622844-C-A

177812903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622839-T-A

177812903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622839-T-C

177812914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622827-T-C

177812938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622818-T-C

http://identifiers.org/hco/4/GRCh38#177813007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53622752-C-A

177813015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53622744-T-G

177813162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622623-T-G

177813214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622581-A-G

177813259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622531-C-G

177813367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622424-T-A

177813525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622263-G-A

177813625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622214-C-T

177813648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622191-G-A

177813648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53622191-G-T

177820708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53621000-A-T

177820863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53620870-T-C

177821042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53620703-A-G

177821284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53620483-A-G

177821319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53620448-T-G

177821568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53620197-T-C

177821577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53620187-T-C

177821946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53618071-T-C

177821981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53618064-A-G

177822011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53618034-C-T

177822210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53617835-C-T

177827371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53616544-T-G

177827720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53616215-T-C

http://identifiers.org/hco/4/GRCh38#177833389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53605413-C-A

177833513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53605289-T-C

177834122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53604673-T-C

177834320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53604483-C-T

177834714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53604091-G-A

177834749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53604054-G-A

177834784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53604011-A-G

177835188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53603610-C-G

177835809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53603325-C-T

177836442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53602769-G-C

http://identifiers.org/hco/4/GRCh38#177836638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53602656-A-C

177836638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53602656-A-T

177836644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53602652-T-G

http://identifiers.org/hco/4/GRCh38#177836650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53602646-C-A

177836722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53602573-C-G

177836957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53602330-A-G

177837323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53601964-A-G

177837351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53601899-A-G

177837456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53601788-A-G

177838522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53601208-G-A

http://identifiers.org/hco/4/GRCh38#177838599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53601129-C-A

http://identifiers.org/hco/4/GRCh38#177838609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53601119-C-A

177838643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53601085-C-T

177838670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53601063-C-T

http://identifiers.org/hco/4/GRCh38#177840076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53600348-A-C

177840113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53600293-G-A

177840168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53600239-T-C

177840290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53600140-T-G

177840375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53600081-A-G

177840408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53600047-G-T

177840432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53600011-T-C

177840466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53599976-A-G

177840556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53599894-G-C

177840656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53599794-A-G

177840786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53599665-T-C

177841207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53599258-A-G

177841223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53599240-G-T

http://identifiers.org/hco/4/GRCh38#177841324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53599153-C-A

http://identifiers.org/hco/4/GRCh38#177841460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53599053-C-A

177841461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53599052-A-G

177841663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53598854-G-T

http://identifiers.org/hco/4/GRCh38#177841718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53598802-C-A

177841734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53598786-A-T

177841763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53598758-A-G

177841764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53598757-C-G

177841828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53598685-A-T

177842056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53598467-C-T

177842124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53598417-T-C

177851590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53594799-A-T

http://identifiers.org/hco/4/GRCh38#177851697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53594691-A-C

177851723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53594665-G-A

177851723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53594665-G-C

http://identifiers.org/hco/4/GRCh38#177852228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53594159-A-C

177852665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593738-A-T

http://identifiers.org/hco/4/GRCh38#177853101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53593570-C-A

177853101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593570-C-G

177853119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593552-T-C

177853119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593552-T-G

177853187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593508-C-T

177853343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593368-T-A

177853402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593300-A-G

177853632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593078-T-C

177853636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593075-C-T

177853691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53593025-C-T

177853783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592915-G-C

177853809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592889-G-A

177853820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592878-G-A

177854071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592624-T-C

http://identifiers.org/hco/4/GRCh38#177854084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53592611-C-A

177854084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592611-C-G

177854106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592589-C-T

177854124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592571-G-A

177854129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592566-A-T

177854132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592563-C-T

177854136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592559-A-G

http://identifiers.org/hco/4/GRCh38#177854138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53592557-C-A

177854138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592557-C-T

177854225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592449-T-C

177854280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53592384-T-C

http://identifiers.org/hco/4/GRCh38#177854308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53592348-A-C

http://identifiers.org/hco/4/GRCh38#177854495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53592170-A-C

http://identifiers.org/hco/4/GRCh38#177855046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53590881-C-A

http://identifiers.org/hco/4/GRCh38#177855047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53590880-C-A

177855047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590880-C-T

177855064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590863-T-C

177855071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590855-C-T

177855188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53590738-G-A

177855277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584410-A-G

177855293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584395-A-G

177855329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584360-A-G

177855377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584312-G-A

177855422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584267-T-C

177855444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584236-A-G

177855512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584176-T-C

177855589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584099-A-G

177855612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53584073-C-T

177855727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583969-A-G

177855735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583961-T-C

177856096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583530-G-A

177856098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583528-T-G

177856234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583391-T-C

177856276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583329-G-C

http://identifiers.org/hco/4/GRCh38#177856290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53583315-C-A

177856290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583315-C-T

177856309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583290-A-G

177856448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583153-G-A

177856466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583135-A-G

177856467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583134-T-C

177856505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583099-C-T

177856530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53583072-C-T

177856603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582993-T-C

177856621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582975-C-T

177856626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582970-C-T

177856682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582925-G-A

177856769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582841-A-G

177856818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582794-T-G

177856919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582688-G-T

177856936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582675-G-A

177857029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582590-A-G

177857225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53582398-A-G

177858971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53581682-T-G

177858994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53581660-A-T

http://identifiers.org/hco/4/GRCh38#177859117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53581555-A-C

177859188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53581492-T-C

http://identifiers.org/hco/4/GRCh38#177859295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53581399-C-A

177859326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53581366-T-C

177859506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53579431-A-G

177859526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53579406-A-G

177864172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578262-T-A

177864172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578262-T-C

177864252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578190-G-A

177864333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578112-A-G

177864402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578062-C-G

177864418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578051-C-T

177864448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578021-A-G

177864455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53578014-T-A

177864818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53577636-G-T

177865005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53577450-T-C

177865031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53577428-G-A

177865031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53577428-G-T

177865072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53577387-T-G

http://identifiers.org/hco/4/GRCh38#177865258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53577205-A-C

177865280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53577175-A-G

177871494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53574772-T-C

177871639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53574646-T-A

177872673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53566232-G-A

177872900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53566020-T-A

177872900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53566020-T-G

177872949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565975-G-A

177872956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565968-T-C

177872973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565951-C-T

177873189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565775-C-G

177873189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565775-C-T

177873304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565658-T-A

177873395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565573-G-A

177873395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565573-G-C

177873395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53565573-G-T

177873624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53564949-G-A

http://identifiers.org/hco/4/GRCh38#177873901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53564693-A-C

177873901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53564693-A-T

177873904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53564690-T-C

177882095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53561669-C-T

177882331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53561437-A-G

http://identifiers.org/hco/4/GRCh38#177882721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53560736-A-C

177882762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53560695-C-T

177883185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53560297-C-T

177883212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53560270-T-G

177883306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53560180-T-C

177887281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53559057-A-G

177887281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53559057-A-T

http://identifiers.org/hco/4/GRCh38#177887720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53558666-A-C

177888469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554971-G-T

177888526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554916-G-C

177888526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554916-G-T

177888643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554798-A-G

177888798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554651-C-T

177889743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

177889744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

177889747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

177889751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

http://identifiers.org/hco/4/GRCh38#177906282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53545368-C-A

177907704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53540435-C-T

http://identifiers.org/hco/4/GRCh38#177907750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53540374-C-A

177907792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53540329-G-A

177907792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53540329-G-T

http://identifiers.org/hco/4/GRCh38#177907803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53540319-C-A

177907825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53540302-T-A

http://identifiers.org/hco/4/GRCh38#177907864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53540277-C-A

http://identifiers.org/hco/4/GRCh38#177907897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53540265-C-A

177907897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53540265-C-T

177907909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53540253-G-T

http://identifiers.org/hco/4/GRCh38#177907980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53540183-C-A

177907980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53540183-C-T

http://identifiers.org/hco/4/GRCh38#177907986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53540177-C-A

177908018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53540144-C-T

177908031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53540131-A-G

http://identifiers.org/hco/4/GRCh38#177908312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53539817-A-C

177908325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539804-G-A

177908351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539774-C-T

177908391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539738-C-T

177908452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539688-A-G

177909852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535954-G-A

177909994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535807-G-C

177910037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535776-C-G

177910112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535718-T-C

177910115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535715-C-T

177910419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535430-G-C

177910674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535183-G-A

177910696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535161-T-G

177910740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535118-T-A

177910748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535110-C-G

177910866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534999-A-T

177910878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534987-T-C

177911387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534769-G-A

http://identifiers.org/hco/4/GRCh38#177913660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53533697-C-A

177913788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53533579-C-T

177913903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53533477-A-G

177913919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53533457-T-C

http://identifiers.org/hco/4/GRCh38#177914294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53533060-C-A

177914366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532885-A-G

177914730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532543-A-G

177914829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532434-T-C

177914835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532428-C-T

http://identifiers.org/hco/4/GRCh38#177915349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53531921-A-C

177915349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53531921-A-G

177926716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53524267-T-C

177926774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53524198-A-G

177926779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53524183-T-C

177927111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53523847-A-G

177927539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53523754-T-C

177927698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53523456-C-T

177928291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53522685-C-T

177929022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53522486-T-C

177929636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53521858-A-G

http://identifiers.org/hco/4/GRCh38#177929670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53521815-A-C

177929758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53521738-C-T

177929878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53521556-C-G

177929878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53521556-C-T

177930077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53521367-A-T

177930204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53521242-A-G

177935480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53511407-T-A

177935671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53511226-A-T

177935769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53511143-T-C

177935773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53511139-G-A

http://identifiers.org/hco/4/GRCh38#177935970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53510957-C-A

177935970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510957-C-T

177936490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510441-A-G

177936548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510384-A-G

177936667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510231-A-G

177936667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510231-A-T

http://identifiers.org/hco/4/GRCh38#177936693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53510205-A-C

177936879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510018-A-G

177936897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53509999-C-T

177937176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53509733-G-A

177941704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506821-A-T

177947332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506058-A-T

177947424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505986-T-C

177947489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505917-G-T

177947732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505662-G-A

177947773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505628-C-T

177947790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505611-G-A

177947790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505611-G-T

177947843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505559-T-G

177947954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505446-T-G

177948006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505361-T-A

177948006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505361-T-C

177948012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505355-A-G

177948172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505200-T-C

177948200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505172-T-C

177948316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505059-A-G

http://identifiers.org/hco/4/GRCh38#177948473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53504905-A-C

177948594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504786-A-G

177948702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504683-A-T

177948803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504586-A-G

177948878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504509-C-T

177949179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504240-G-A

177950495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502911-A-G

177950751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502636-T-C

177950973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502421-A-G

177951242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502165-T-C

177951380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501989-A-G

177951647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501586-G-A

177951981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501242-T-C

177952257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53500976-G-A

177952592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53500650-T-A

177952592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53500650-T-C

177952674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499673-C-T

177952908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499430-C-G

177952976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499362-A-G

177953186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499198-T-C

177953205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499171-C-T

177953278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499091-A-G

177953377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498987-G-T

177953437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498929-G-T

177953854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498546-A-G

177954007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498414-A-G

177956975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494182-G-A

177957039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494138-G-A

177957039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494138-G-C

177957105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494087-C-T

177957303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493900-G-A

177957413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493804-C-T

177957486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493760-C-T

177957635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493600-G-A

177957686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493553-G-A

177957706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493539-T-C

177957855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493405-A-G

177957861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493399-A-G

177958174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493164-C-T

177959085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492366-C-T

177959198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492255-A-G

177959210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492239-G-C

177959446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492025-A-G

177959552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491920-C-T

177959744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491752-A-G

177959844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491654-C-T

177959885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491643-C-T

177959924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491640-C-T

177960125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491468-A-G

177960236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491348-C-T

177960283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491291-T-C

http://identifiers.org/hco/4/GRCh38#177960558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53491014-A-C

177960634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490937-G-T

177960640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490931-T-A

177960640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490931-T-C

177960640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490931-T-G

177960670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490901-A-G

177960672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490899-A-G

177960672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490899-A-T

http://identifiers.org/hco/4/GRCh38#177960713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53490859-C-A

http://identifiers.org/hco/4/GRCh38#177960720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53490852-C-A

177960720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490852-C-T

http://identifiers.org/hco/4/GRCh38#177960754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53490821-C-A

177960754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53490821-C-T

177960812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53490784-T-C

177960821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53490775-T-C

177960838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53490758-A-G

http://identifiers.org/hco/4/GRCh38#177960850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53490746-A-C

177960850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53490746-A-G

177960853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53490743-A-G

177960854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53490742-A-G

177960893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: non coding transcript exon variant
orthologous variants: 53490704-C-T

177960910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53490688-G-A

177960932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53490666-T-C

177960988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53490606-T-C

177960988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53490606-T-G

http://identifiers.org/hco/4/GRCh38#177961040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53490553-C-A

177961040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53490553-C-T

177961419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490112-T-A

177961512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490016-G-T

177961598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489928-G-A

177963340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489817-T-C

177963611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489531-T-C

http://identifiers.org/hco/4/GRCh38#177964267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#53488843-A-C

177964421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488694-G-A

177964421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488694-G-C

177964421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488694-G-T

177964445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488670-T-A

177964778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53487701-T-G

http://identifiers.org/hco/4/GRCh38#177964865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53487616-A-C

177964882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487602-A-T

177964989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487493-G-A

177964996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53487488-T-C

177965009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53487475-A-G

177965146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53487356-T-C

177965163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487339-G-A

177965233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487286-C-G

177965443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487173-T-G

http://identifiers.org/hco/4/GRCh38#177965714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53486908-A-C

177965753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486869-T-C

177966094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486516-A-G

177966111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486501-T-A

177966112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486500-A-G

177966252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486347-T-G

177969143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476684-A-G

177969422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476366-T-C

177969423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476365-G-A

177969517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476269-G-A

177969517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476269-G-T

177971120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53474333-T-C

177971176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53474272-G-T

177971311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53474137-G-A

177971330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53474118-C-G

177971445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53474001-A-G

177971784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53473676-T-A

177971784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53473676-T-C

177971866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53473592-T-G

177972118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53473354-T-C

177972161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53473311-A-T

177972284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53473156-A-G

177972644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472775-G-A

177972685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472733-G-T

http://identifiers.org/hco/4/GRCh38#177972706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53472716-A-C

177972739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472683-C-G

177972739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472683-C-T

http://identifiers.org/hco/4/GRCh38#177974706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53470263-A-C

177974777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470185-A-G

http://identifiers.org/hco/4/GRCh38#177975193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53469789-C-A

177975248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53469739-C-T

177975678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53469312-A-G

177975684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53469306-G-T

177975708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53469282-T-C

177976137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468858-T-G

177976469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468301-A-G

177976504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468266-A-G

177976679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468089-C-G

http://identifiers.org/hco/4/GRCh38#177976911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53467856-C-A

177976914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467853-T-C

177977034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467735-T-C

177977379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467077-G-T

177977398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467058-A-G

177977827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466618-G-A

177977827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466618-G-T

177978075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465450-T-C

177978316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465232-G-A

177978419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465143-T-C

177981395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463932-T-G

177982238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463083-G-A

177982390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462928-T-C

177982454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462867-A-G

177982617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462737-C-G

177982617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462737-C-T

177983098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462216-G-A

177983495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461802-A-G

177983560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461737-G-A

177983658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461687-T-C

177983736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461612-T-C

177983801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461576-T-C

177983853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461526-A-G

177984757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458885-G-C

177984769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458873-A-G

177984847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458798-T-C

177984927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458730-T-C

177985039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458560-G-A

177986263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53457941-G-A

177986329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53457874-A-G

177986448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53457758-G-A

177986561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53457659-G-A

177987577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53453812-A-G

177987663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53453723-C-T

177987845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53453551-C-T

177990140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53452407-G-A

177990158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53452389-G-C

177990186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53452357-C-T

177990259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53452289-A-G

177990337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53452213-G-A

177990448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53452107-A-G

177990495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53452073-C-T

177990571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53452001-G-A

177990826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53451748-T-C

http://identifiers.org/hco/4/GRCh38#177990890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53451684-C-A

177990930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53451646-T-C

177990930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53451646-T-G

177991488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449899-A-G

177991632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449758-A-G

177991806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449587-T-C

177991876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449512-C-T

177992197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449064-T-A

177992203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449058-G-A

177992209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449052-C-T

177992230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53449008-C-T

177992462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53448557-C-G

177992527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53448492-A-G

http://identifiers.org/hco/4/GRCh38#177992613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53448408-C-A

177992861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53448231-C-T

177992967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53448125-T-C

177993372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53447747-C-T

177997516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53447314-A-G

177997541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53447287-T-C

177997561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53447269-A-T

177997646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53447187-T-C

177997719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53447114-A-T

177997770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53447078-C-T

177998001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53446857-T-G

http://identifiers.org/hco/4/GRCh38#177998094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53446768-A-C

177998229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53446672-T-C

177998298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53446606-G-A