http://identifiers.org/hco/3/GRCh38#157543350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#66250353-C-A

157543350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250353-C-G

http://identifiers.org/hco/3/GRCh38#157543353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#66250356-C-A

157543353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250356-C-T

157543357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250361-C-T

157543359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250363-C-G

157543359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250363-C-T

157543362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250366-G-A

157543362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250366-G-T

157543374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66250371-T-C

http://identifiers.org/hco/3/GRCh38#157543398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66250391-C-A

157543408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66250401-G-A

157543408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66250401-G-T

157543515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66250541-T-C

157543586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66250610-C-T

157543599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66250623-G-T

157543642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66250670-A-G

157544333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66251510-G-A

157544356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66251579-T-G

157544483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66251761-A-G

157544491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66251769-C-T

157544731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66251975-T-G

157544745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66251989-A-G

157544837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252074-T-C

157544899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252096-G-C

http://identifiers.org/hco/3/GRCh38#157544942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66252139-C-A

157545332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252597-T-A

http://identifiers.org/hco/3/GRCh38#157545363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66252623-A-C

http://identifiers.org/hco/3/GRCh38#157545473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66252720-A-C

157545495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252741-T-C

157545609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252856-G-A

http://identifiers.org/hco/3/GRCh38#157545640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66252888-C-A

157570875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270921-A-G

157571842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271498-G-A

157571842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271498-G-T

http://identifiers.org/hco/3/GRCh38#157571937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66271942-C-A

157571945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271949-A-G

157571945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271949-A-T

http://identifiers.org/hco/3/GRCh38#157571965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66271969-C-A

157571965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271969-C-G

157571965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271969-C-T

http://identifiers.org/hco/3/GRCh38#157571972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66271976-C-A

157571972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271976-C-G

157571972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271976-C-T

157571980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271984-A-G

http://identifiers.org/hco/3/GRCh38#157571983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66271987-C-A

157571983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271987-C-T

http://identifiers.org/hco/3/GRCh38#157571993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66271997-C-A

157571993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271997-C-G

157571993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66271997-C-T

http://identifiers.org/hco/3/GRCh38#157572066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66272070-C-A

157572066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272070-C-G

157572066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272070-C-T

157572141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272145-T-A

157572141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272145-T-C

http://identifiers.org/hco/3/GRCh38#157572162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66272167-A-C

157572162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272167-A-G

157572162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272167-A-T

157572507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272492-A-G

157572558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272540-C-T

157572714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272700-C-T

157572724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272710-G-A

157572724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272710-G-T

157572902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272877-C-T

157572986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272955-T-A

157573029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272986-G-A

157573153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66273091-G-T

157573678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66273556-T-A

157573780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66273637-C-T

157573895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66273751-G-C

157574040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66274635-G-A

157574040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66274635-G-C

157574464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66274989-T-C

157574465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66274990-C-T

157574561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275081-T-A

157574692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275198-T-C

157574788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275270-A-G

157574990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275468-A-G

157575028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275503-G-A

157575157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66275621-G-A

157575157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66275621-G-T

157575428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275864-T-C

157575608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66276051-G-C

http://identifiers.org/hco/3/GRCh38#157575697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66276140-C-A

157575797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66276242-G-A

157576002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66276448-A-G

157576367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66276806-A-G

157576372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66276811-T-C

157576689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66277106-C-T

157578314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66279941-G-A

157578314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66279941-G-T

157578316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66279943-T-A

http://identifiers.org/hco/3/GRCh38#157578426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66280017-C-A

157578426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280017-C-T

157578459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280048-T-A

157578550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280102-T-A

157578622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280161-T-C

157578622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280161-T-G

157578676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280215-G-A

http://identifiers.org/hco/3/GRCh38#157578706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66280249-C-A

157578712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280255-T-C

157578712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280255-T-G

157578722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280266-A-T

http://identifiers.org/hco/3/GRCh38#157578740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66280278-C-A

157578740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280278-C-T

157578744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280282-G-A

157578744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66280282-G-T

157578940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66280465-T-C

http://identifiers.org/hco/3/GRCh38#157578995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66280520-C-A

157578995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66280520-C-G

157578995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66280520-C-T

157588631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66280826-T-C

157588790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66281060-A-G

157589361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66281496-T-C

http://identifiers.org/hco/3/GRCh38#157589667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66281808-C-A

157589667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66281808-C-T

157589828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66281972-A-G

157589866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66282010-A-G

157590169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66282310-C-T

157590289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66282437-G-C

157590414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66282595-C-T

http://identifiers.org/hco/3/GRCh38#157592893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66284593-C-A

157593510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66285628-A-G

157593548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66285669-T-C

157593587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66285708-C-T

157593668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66285951-T-C

157593735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66286144-A-G

157594755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66287084-T-C

157594917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66287168-G-T

157594925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66287176-C-G

157595020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66287274-G-A

http://identifiers.org/hco/3/GRCh38#157595042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66287299-A-C

157595042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66287299-A-T

157595232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66287461-T-A

157595232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66287461-T-C

http://identifiers.org/hco/3/GRCh38#157595274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66287504-A-C

157595687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66288480-G-C

http://identifiers.org/hco/3/GRCh38#157595767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66288545-C-A

157595975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66288784-T-C

http://identifiers.org/hco/3/GRCh38#157596226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66288792-C-A

157596607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66289172-T-C

http://identifiers.org/hco/3/GRCh38#157597301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66289864-C-A

157597384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66289945-G-T

157597533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66290081-T-C

157597665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66290209-G-A

157597665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66290209-G-T

157597848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66290338-T-C

http://identifiers.org/hco/3/GRCh38#157597986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66290471-A-C

157598507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66290943-A-G

http://identifiers.org/hco/3/GRCh38#157599095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66291359-C-A

157599366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66291835-T-G

157599504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66292162-A-G

157599553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66292210-A-G

157599565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66292222-A-G

157599697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66292336-G-T

157599714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66292353-A-G

157600923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292627-G-A

157600923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292627-G-T

http://identifiers.org/hco/3/GRCh38#157600925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66292629-C-A

http://identifiers.org/hco/3/GRCh38#157600934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66292634-C-A

157600934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292634-C-T

157600936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292636-G-A

157600936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292636-G-T

157600966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292666-G-A

157600966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292666-G-T

157601076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292736-A-G

157601165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292804-A-T

157601187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66292826-G-T

157601313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66292942-C-T

157601906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66294053-A-G

157601996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66302547-G-C

http://identifiers.org/hco/3/GRCh38#157602605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66303129-A-C

157602872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66303376-A-G

157603473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66304402-G-C

157604042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66304578-T-G

157604260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66304732-C-G

157604290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66304764-A-G

157604434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66304993-G-A

157605765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66305310-C-T

157605995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66305595-A-G

157606409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66305995-C-T

http://identifiers.org/hco/3/GRCh38#157606425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66306011-C-A

157606449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66306035-G-C

157606815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66306394-C-G

157606912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66306495-G-A

157606978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66306563-G-C

157607022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66306660-T-C

157607550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66307236-C-T

157608099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66308510-G-C

157608174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66308586-G-A

157608725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309136-A-G

157609088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309429-C-G

157609088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309429-C-T

157609089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309430-G-A

157609403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309790-T-C

157609700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310075-C-T

157609727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310102-G-C

157610421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310740-C-T

157610458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310783-C-T

157610578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310879-G-A

157610825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311112-G-A

157611945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312089-C-G

157612241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312560-A-G

http://identifiers.org/hco/3/GRCh38#157612297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66312616-A-C

157612509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312865-G-C

157612689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313020-G-C

http://identifiers.org/hco/3/GRCh38#157613066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66313491-C-A

157613066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313491-C-T

157613172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313626-T-G

http://identifiers.org/hco/3/GRCh38#157613240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66313688-A-C

157613240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313688-A-G

157613541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313984-G-T

157613623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314054-A-G

157613713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314135-C-T

http://identifiers.org/hco/3/GRCh38#157613847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66314268-C-A

157613866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314287-T-C

157613873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314294-T-C

157613987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314410-G-C

157615937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66315730-A-G

157616048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66315831-A-G

157616432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316187-G-A

157616432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316187-G-C

157616439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316194-C-T

157616626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316373-G-T

157616948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316660-T-C

157617096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316773-G-T

http://identifiers.org/hco/3/GRCh38#157617181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66316854-C-A

157617824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317741-T-C

157617857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317770-T-C

157617877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317790-G-A

157617918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317829-T-C

157617922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317833-G-C

157617936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317847-T-C

157618014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66317911-A-G

157618014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66317911-A-T

157618041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317940-C-T

157618082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66317981-A-G

157618085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66317984-G-A

157618144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66318045-T-C

http://identifiers.org/hco/3/GRCh38#157618520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66318463-C-A

157618672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318603-G-A

157618820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318752-T-C

http://identifiers.org/hco/3/GRCh38#157619034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66318974-C-A

157619182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319098-C-G

157619513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319436-C-T

157619584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319509-G-T

http://identifiers.org/hco/3/GRCh38#157619707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66319636-C-A

157619775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319728-G-A

http://identifiers.org/hco/3/GRCh38#157619932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66319883-C-A

157619932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319883-C-T

157619987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319938-G-A

http://identifiers.org/hco/3/GRCh38#157620290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66320247-A-C

157620290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320247-A-G

157620324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320281-T-C

157620325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320282-A-G

157620538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320518-G-A

157620586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320566-A-G

157620681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320660-T-C

157620876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320828-A-G

http://identifiers.org/hco/3/GRCh38#157622645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66321230-A-C

http://identifiers.org/hco/3/GRCh38#157622751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66321340-C-A

157622777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321366-A-G

157622808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321397-G-T

157622900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321473-C-T

157622933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321506-A-G

157623140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321716-T-C

157623206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322213-A-G

157623227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322234-G-A

157623321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322315-A-G

157623641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322625-C-G

157624588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66323275-T-G

157624800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66323489-A-T

157624955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66323583-A-G

157625406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324006-T-A

http://identifiers.org/hco/3/GRCh38#157625577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66324226-C-A

157625835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324460-A-G

http://identifiers.org/hco/3/GRCh38#157625911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66324511-C-A

157626022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324607-T-C

157626136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324714-G-A

157626283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324857-A-G

157626344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324918-C-G

157626375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324949-G-A

157626611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325277-A-G

157626662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325346-G-A

http://identifiers.org/hco/3/GRCh38#157626805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66325571-C-A

157626805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325571-C-G

157629067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327281-T-C

157629134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327348-T-A

157629135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327349-T-C

157629605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327745-G-A

157629796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327935-A-G

157630036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328104-G-T

157630113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328149-A-G

157630399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328416-T-C

157630425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328436-G-C

157630589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328586-T-C

157630618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328615-A-G

157630683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328676-T-C

157630722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328715-G-C

157630746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66328800-G-T

157631097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329141-G-C

157631319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329345-G-A

157631353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329377-T-G

157631417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329419-G-A

157631658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329653-C-T

157631659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329654-G-A

157631659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329654-G-T

157631664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329659-C-T

157631714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329707-G-T

157632432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330483-A-G

157632847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331007-T-A

157632847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331007-T-C

157632865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331025-T-G

157632867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331027-A-G

157632967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331091-G-T

157632998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331144-A-G

157633034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331171-G-A

157633144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331274-C-T

157633227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331322-G-A

157633469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331554-G-A

157633734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331824-T-A

157633826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331916-T-C

157635177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66333942-C-T

157635450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334192-T-C

157636015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334747-G-A

157636183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334954-G-A

157636187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334958-A-G

157636189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334960-A-T

157638291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66346211-C-T

157638321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66346241-A-G

157639823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66348367-G-A

157640020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66348555-G-C

157640174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66348710-T-C

157640313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66348847-T-C

157640831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66349336-T-C

157641383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66349857-T-C

http://identifiers.org/hco/3/GRCh38#157641666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66350156-A-C

157641873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66350515-G-A

157641990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66350604-A-G

157642015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66350629-G-A

157642015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66350629-G-C

157642184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66350793-A-T

157642680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66351247-T-C

157643191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66351811-C-T

157643202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66351828-G-A

157643306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66351920-A-G

157643517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66352118-G-C

157644147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66353167-A-T

157644426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66353436-C-T

http://identifiers.org/hco/3/GRCh38#157644712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66353714-C-A

157644717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66353719-T-C

157645313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354264-C-G

157645534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354614-T-C

157645540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354620-C-G

157645540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354620-C-T

157645654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354696-G-A

157645654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354696-G-T

157645661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354703-C-T

157645732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354765-G-T

http://identifiers.org/hco/3/GRCh38#157645806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66354823-A-C

157645830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66354845-T-A

157645834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66354849-G-A

157646020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66355004-G-T

157647012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66356698-G-A

157647031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66356714-C-G

157647184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66356840-T-C

157647274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66356919-G-A

157647292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66356937-A-G

157647325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66356969-G-A

157647385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66357026-A-T

157647421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66357060-C-G

157647742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66357351-G-T

157648346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364489-C-G

157648346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364489-C-T

157648348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364491-C-T

157648361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364503-G-A

157648486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364628-C-T

157648492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364634-A-G

157648548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364692-G-A

http://identifiers.org/hco/3/GRCh38#157649031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66364800-A-C

http://identifiers.org/hco/3/GRCh38#157649119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66364884-A-C

157649136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364902-A-T

157649215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66364964-A-T

157649523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365296-G-A

http://identifiers.org/hco/3/GRCh38#157649540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66365313-C-A

157649540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365313-C-G

157649541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365314-A-T

157649579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365350-G-C

157649585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365356-G-A

http://identifiers.org/hco/3/GRCh38#157649722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66365476-C-A

157649731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365485-T-A

157649780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365533-T-C

157649811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365563-C-G

157650005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365725-T-A

157650211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365906-A-G

http://identifiers.org/hco/3/GRCh38#157650268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66365964-C-A

157650287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66365982-C-G

157650498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366203-G-C

http://identifiers.org/hco/3/GRCh38#157650559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66366264-C-A

157650564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366269-C-T

157650577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366282-A-G

157650583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366288-C-T

157650594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366299-C-T

157651464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366384-C-T

157651496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366412-T-C

157651581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366497-T-C

157651667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366579-C-T

157651902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66366794-G-A

157651968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367344-G-A

157652167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367505-G-A

157652372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367710-C-T

157652378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367716-T-C

157652435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367772-T-C

157652511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367841-G-T

157652512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367842-G-A

157652512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66367842-G-C

http://identifiers.org/hco/3/GRCh38#157653247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66368365-C-A

157653247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66368365-C-T

157653406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66368555-G-T

157653435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66368584-T-C

http://identifiers.org/hco/3/GRCh38#157653447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66368596-A-C

157653539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66368692-T-C

157653693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66368842-G-A

157653777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66368918-G-A

157653818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66368956-G-T

157653924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66369068-T-C

157654148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66369236-T-C

157654214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66369298-G-A

157654316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66369403-T-C

157654499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66369531-T-G

http://identifiers.org/hco/3/GRCh38#157655271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66370221-C-A

157655271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66370221-C-T

157655280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66370230-A-T

157657146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66370499-G-T

http://identifiers.org/hco/3/GRCh38#157657347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66370641-A-C

157658137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371028-G-A

157658137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371028-G-T

157658264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371118-G-C

157658397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371272-G-A

157658630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371600-A-G

157658830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371699-A-G

157658915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371781-T-C

157659103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66371964-T-G

157659323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66372093-C-T

157659475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66372198-A-G

157659506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66372229-A-G

157661022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66373893-T-A

157661184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66374054-T-C

157661404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66374278-G-C

157662746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66375336-G-T

157663862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66375603-A-T

157664201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66376200-T-C

157664239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66376246-T-C

157665139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66377205-A-T

157665198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66377252-G-C

157665878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66378056-T-G

157667078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66378526-C-T

157667091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66378537-T-C

157667147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66378592-C-T

157667532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66378883-T-C

157667552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66378906-C-T

http://identifiers.org/hco/3/GRCh38#157667604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66378958-C-A

157667604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66378958-C-T

157668572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385972-C-T

157668661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386037-G-A

157668968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386309-T-C

157669232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386567-G-A

157669245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386580-A-G

157670270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387602-G-A

157670380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387712-T-C

157670688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387954-C-T

157670714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387973-G-A

157671528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388077-A-G

157671812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388356-C-T

157671937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388483-G-A

157672101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388649-T-C

157672178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388717-G-T

157672338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388847-T-C

157672344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388852-A-G

157672530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66389037-C-T

157674952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390137-T-C

157674958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390143-T-G

157674970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390155-T-C

157675482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390456-G-A

157675482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390456-G-T

157675662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390625-C-G

http://identifiers.org/hco/3/GRCh38#157676099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66391057-A-C

157676172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391127-A-G

157676269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391228-A-G

157676369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391329-A-G

157676475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391437-A-T

157676526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391485-T-C

157676555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391514-G-A

157676722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391678-G-A

157676760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391717-C-T

157676820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391776-C-T

157676953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391879-C-T

157677042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391978-C-G

157677163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392101-C-G

http://identifiers.org/hco/3/GRCh38#157677171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66392109-C-A

157677237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392177-T-C

157677239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392179-G-A

157677395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392316-T-C

157677434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392355-G-C

http://identifiers.org/hco/3/GRCh38#157677459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#66392381-A-C

157677459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392381-A-G

157677493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392414-A-G

157677537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66392458-G-A

157677537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66392458-G-C

157677590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66392512-G-T

157677619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66392541-G-A

157677642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66392563-G-C

157677656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66392577-G-A

157677721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25146
most severe consequence: non coding transcript exon variant
orthologous variants: 66392646-G-T