160453468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12637969-G-A

160453477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12637960-A-G

http://identifiers.org/hco/6/GRCh38#160453501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12637936-C-A

160453501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12637936-C-T

160453543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12637894-T-C

160454237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12637654-G-A

160454267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12637624-T-C

160454297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12637594-T-C

160454350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637542-G-T

160454356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637536-C-T

160454415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637486-G-A

160454415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637486-G-T

160454445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637457-G-T

160454452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637450-T-C

160454536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637369-A-G

160454536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12637369-A-T

160455019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12636349-G-A

160455185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12636162-C-T

160455186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12636161-G-A

http://identifiers.org/hco/6/GRCh38#160455197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12636152-C-A

160455311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12636053-T-C

160455648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635650-T-A

160455648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635650-T-G

160455735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635561-G-A

160455845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635467-G-A

160456099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635333-A-G

160456120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635315-A-G

160456170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635264-G-A

160456170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635264-G-C

160456214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635222-G-C

160456264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12635146-G-A

160456347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12635066-G-A

160456750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12634925-T-C

160456750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12634925-T-G

160457773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12634076-T-G

160458015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12633761-G-A

160458533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12633552-A-G

160458698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12633401-G-T

160458810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12633361-T-C

160458851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12633340-G-A

160459174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12633051-G-T

160459214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632996-G-T

160459219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632991-T-C

http://identifiers.org/hco/6/GRCh38#160459224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12632986-C-A

160459224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632986-C-T

160459261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632949-G-A

160459261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632949-G-T

http://identifiers.org/hco/6/GRCh38#160459279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12632931-C-A

160459279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632931-C-G

http://identifiers.org/hco/6/GRCh38#160459285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12632925-C-A

160459285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632925-C-T

160459309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632904-T-C

http://identifiers.org/hco/6/GRCh38#160459542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12632477-C-A

160459542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632477-C-T

http://identifiers.org/hco/6/GRCh38#160459582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12632430-C-A

160459583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632429-C-T

160459584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632428-A-G

160459768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632233-A-G

160459961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12632011-C-G

160459987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12631983-G-A

160460091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12631881-C-T

160460378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12629229-C-T

160460428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12629184-T-C

160460632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12628612-A-G

http://identifiers.org/hco/6/GRCh38#160460709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12628540-C-A

160460709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12628540-C-T

160461151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12628088-G-T

http://identifiers.org/hco/6/GRCh38#160461168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12628072-A-C

160461168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12628072-A-G

160461199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12628049-A-G

160461204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12628044-G-A

160461204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12628044-G-T

160461292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12627961-G-A

160461292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12627961-G-C

160461292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12627961-G-T

160461315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12627938-A-G

160461318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12627935-C-T

160461333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12627920-T-C

http://identifiers.org/hco/6/GRCh38#160461401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12627852-C-A

160461401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627852-C-T

160461402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627851-G-A

160461402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627851-G-T

160461409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627845-A-G

160461409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627845-A-T

160461437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627807-T-C

160461527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627734-G-C

160461527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627734-G-T

160461548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627713-C-T

160461633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627648-C-T

160461668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627613-G-C

160461678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627603-A-G

http://identifiers.org/hco/6/GRCh38#160461936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12627226-C-A

160461965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627194-G-A

160461979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12627180-T-C

160462939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12625812-G-T

160463002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12625762-A-G

160463031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12625737-A-T

http://identifiers.org/hco/6/GRCh38#160463207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12625511-A-C

http://identifiers.org/hco/6/GRCh38#160463404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12625351-C-A

160463983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12624403-T-C

http://identifiers.org/hco/6/GRCh38#160464091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12624328-C-A

160464091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12624328-C-T

160464133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12624294-T-C

160464346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12624017-G-A

160464346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12624017-G-T

160464571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12623846-G-A

http://identifiers.org/hco/6/GRCh38#160466909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12623006-A-C

160466909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12623006-A-G

160466918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622997-T-C

160466924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622991-T-A

160466924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622991-T-C

160466972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622943-G-A

160466972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622943-G-C

160466972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622943-G-T

160467235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622435-G-T

160467351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622303-T-A

160467351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622303-T-C

160467351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622303-T-G

160467422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622234-G-A

http://identifiers.org/hco/6/GRCh38#160467435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12622221-C-A

160467435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622221-C-T

160467444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622213-T-A

160467444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622213-T-C

160467462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622196-G-T

160467468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622190-G-A

160467468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622190-G-T

160467470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622188-A-G

http://identifiers.org/hco/6/GRCh38#160467507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12622154-C-A

160467630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622025-C-G

160467630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622025-C-T

160467669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12621986-C-T

160467755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621901-G-A

160467778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12621890-G-C

160467778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12621890-G-T

160467815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621850-G-A

160467815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621850-G-T

160468975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621508-G-A

160469107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621386-C-G

160469107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621386-C-T

160469360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621173-G-A

160469391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621135-C-T

160469532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621001-G-T

160476968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617292-T-C

160477008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617252-T-C

160477261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12617005-C-T

160477331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616927-G-A

160477349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616909-T-G

160477448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616788-C-T

http://identifiers.org/hco/6/GRCh38#160477661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12616611-C-A

160478475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622154-A-G

160478599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622025-C-T

160478638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12621986-C-G

160478665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12621959-C-T

160482830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616964-A-G

160482831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616963-A-G

160482867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616927-G-A

160482867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616927-G-T

160482885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616909-T-G

160483149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616658-T-A

160483216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616619-G-A

160483217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616618-G-A

160483217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616618-G-T

160483224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616611-C-G

160483275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616556-G-T

160483985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622196-G-A

160483991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622190-G-A

http://identifiers.org/hco/6/GRCh38#160484195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12621986-C-A

160484195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12621986-C-T

http://identifiers.org/hco/6/GRCh38#160484222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12621959-C-A

160485947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12617005-T-A

160487132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622234-T-C

160487172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622196-G-A

160487172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622196-G-C

160487172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622196-G-T

160487178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622190-G-C

160487180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12622188-A-G

160487343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622025-C-G

160487343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12622025-C-T

http://identifiers.org/hco/6/GRCh38#160487382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12621986-C-A

160487382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12621986-C-T

160488142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621342-G-A

160491493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12617005-T-G

160491914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616619-G-A

160491915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616618-G-A

160491915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616618-G-T

http://identifiers.org/hco/6/GRCh38#160491922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12616611-C-A

160491922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616611-C-T

160491973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616556-G-T

http://identifiers.org/hco/6/GRCh38#160492676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12622221-C-A

160492676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622221-C-G

http://identifiers.org/hco/6/GRCh38#160492702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12622196-C-A

160492708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622190-G-A

160492708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622190-G-T

160492710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622188-A-G

160493005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621894-T-C

160493021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621890-G-A

160500498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617421-G-A

160500498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617421-G-T

160500913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non coding transcript exon variant
orthologous variants: 12617005-T-C

160501035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616880-A-G

160510409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598118-C-T

160510852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12597712-G-T

160510936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12597632-A-G

160510936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12597632-A-T

http://identifiers.org/hco/6/GRCh38#160510941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#12597627-A-C

160519655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590775-G-C

160519662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590768-C-G

160519731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12590701-T-C

160520036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21210
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 12590393-G-T