16474416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140761792-C-G

http://identifiers.org/hco/1/GRCh38#16474420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761796-A-C

16474420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140761796-A-T

16474675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762038-A-G

16475660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762316-G-A

16475696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762352-A-G

http://identifiers.org/hco/1/GRCh38#16475727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762383-C-A

16475727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762383-C-T

http://identifiers.org/hco/1/GRCh38#16475746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762402-C-A

16475754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762410-G-A

16475754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762410-G-T

16475768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762424-G-A

16475768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762424-G-T

16475807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762446-A-G

16475807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762446-A-T

http://identifiers.org/hco/1/GRCh38#16475830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762469-C-A

http://identifiers.org/hco/1/GRCh38#16475879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762518-C-A

16475879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762518-C-G

16475879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762518-C-T

http://identifiers.org/hco/1/GRCh38#16475882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762521-C-A

16475882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762521-C-T

16475888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762527-T-A

16475888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762527-T-C

http://identifiers.org/hco/1/GRCh38#16475911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762550-C-A

16475911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762550-C-T

http://identifiers.org/hco/1/GRCh38#16475927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762566-C-A

16475927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762566-C-T

http://identifiers.org/hco/1/GRCh38#16475972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762611-C-A

16475972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762611-C-T

16475990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762629-T-A

16475990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762629-T-C

http://identifiers.org/hco/1/GRCh38#16475995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762634-C-A

16475995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762634-C-G

16475995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762634-C-T

16476031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762670-G-A

16476031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762670-G-T

16476047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762686-T-C

16476047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140762686-T-G

16476077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762708-G-A

16476077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762708-G-C

16476085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762716-G-T

http://identifiers.org/hco/1/GRCh38#16476136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762767-C-A

16476136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762767-C-T

16476157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762791-T-C

http://identifiers.org/hco/1/GRCh38#16476181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762815-C-A

16476181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762815-C-T

16476306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762930-G-A

16476306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762930-G-T

16476307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762931-G-A

16476307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762931-G-T

16476405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140763004-G-T

http://identifiers.org/hco/1/GRCh38#16476407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763006-C-A

16476407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140763006-C-T

16476468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140763067-C-G

16476468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140763067-C-T

16476511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140763176-G-T

16476530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763246-G-C

http://identifiers.org/hco/1/GRCh38#16476589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763346-C-A

16476589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763346-C-T

http://identifiers.org/hco/1/GRCh38#16476614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763403-C-A

http://identifiers.org/hco/1/GRCh38#16476641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763431-C-A

16476715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763518-G-A

http://identifiers.org/hco/1/GRCh38#16476821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763737-C-A

16476821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763737-C-T

16476836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763752-T-A

16476836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763752-T-C

16476868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763805-G-T

16476877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763814-T-C

http://identifiers.org/hco/1/GRCh38#16476927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763992-C-A

http://identifiers.org/hco/1/GRCh38#16477059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140764124-C-A

16477059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140764124-C-T

http://identifiers.org/hco/1/GRCh38#16477120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140764171-C-A

16477159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140764209-C-T

16477177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140764228-T-C

http://identifiers.org/hco/1/GRCh38#16477213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140764265-C-A

16477213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140764265-C-G

16477240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140764288-G-A

16477919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140764838-A-T

http://identifiers.org/hco/1/GRCh38#16477940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140764859-A-C

16477949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140764868-G-A

http://identifiers.org/hco/1/GRCh38#16478161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765072-A-C

16478161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765072-A-G

16478161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765072-A-T

16478163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765074-G-A

16478163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765074-G-C

16478163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765074-G-T

http://identifiers.org/hco/1/GRCh38#16478166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765077-C-A

16478191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765106-G-A

16478191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765106-G-T

http://identifiers.org/hco/1/GRCh38#16478228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765135-C-A

16478228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765135-C-T

16478229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765136-T-A

16478229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765136-T-C

16478229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765136-T-G

16478239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765146-G-A

16478239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765146-G-T

16478241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765148-G-A

16478241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765148-G-C

16478241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140765148-G-T

16478280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765184-G-A

16478280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765184-G-C

16478280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765184-G-T

http://identifiers.org/hco/1/GRCh38#16478320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765224-C-A

16478320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765224-C-G

16478320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765224-C-T

16478324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765228-T-A

16478324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765228-T-C

16478332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765236-G-A

16478332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765236-G-T

http://identifiers.org/hco/1/GRCh38#16478377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765281-C-A

16478377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765281-C-T

http://identifiers.org/hco/1/GRCh38#16478378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765282-C-A

16478378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765282-C-G

16478378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765282-C-T

16478388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140765292-T-C

http://identifiers.org/hco/1/GRCh38#16478437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765341-C-A

16478437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 140765341-C-T

16478479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765394-G-T

http://identifiers.org/hco/1/GRCh38#16478489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765404-C-A

16478489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765404-C-T

16478531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765428-A-G

16478531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765428-A-T

16478667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765571-C-T

16478725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765630-T-G

16478911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765783-G-A

16480238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765947-G-A

16480364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140766058-T-C

16480386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140766078-A-G

16480426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140766105-A-G

16480499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140766177-G-A

16480570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140766244-A-G

16483229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768222-T-C

http://identifiers.org/hco/1/GRCh38#16483257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768242-C-A

16483268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768253-G-A

16483268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768253-G-T

16483274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768259-A-T

16483277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768262-T-C

16483277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768262-T-G

http://identifiers.org/hco/1/GRCh38#16483281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768266-C-A

16483281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768266-C-G

16483281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768266-C-T

16483442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140768426-G-A

16483582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768534-G-A

16483582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768534-G-T

16483660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768566-T-C

16483680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768589-C-T

16483702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768611-G-A

16483759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768641-T-C

16483769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768651-G-A

16483769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768651-G-T

16483793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768673-C-T

16483811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768691-G-T

http://identifiers.org/hco/1/GRCh38#16483823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768708-C-A

16483988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768823-C-T

16484014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768849-T-C

16484142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768895-G-A

16484142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768895-G-C

16484142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768895-G-T

http://identifiers.org/hco/1/GRCh38#16484188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768916-C-A

16484188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768916-C-T

http://identifiers.org/hco/1/GRCh38#16484228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768929-C-A

16484228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140768929-C-T

16484287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140768988-G-A

16484287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140768988-G-T

16484305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769006-G-A

16484305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769006-G-C

16484305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769006-G-T

16484326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769027-A-G

http://identifiers.org/hco/1/GRCh38#16484362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769060-C-A

16484362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769060-C-G

16484362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769060-C-T

16484365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769063-G-A

16484365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769063-G-T

16484374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769072-G-A

16484374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769072-G-T

16484382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769080-G-A

16484382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769080-G-C

16484382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769080-G-T

http://identifiers.org/hco/1/GRCh38#16484386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769084-C-A

16484386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140769084-C-T

16484480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769175-G-A

16484480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769175-G-C

16484480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769175-G-T

16484517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769194-G-A

16484517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769194-G-T

http://identifiers.org/hco/1/GRCh38#16484522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769199-C-A

16484522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769199-C-T

16484554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769215-G-A

16484554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769215-G-T

http://identifiers.org/hco/1/GRCh38#16484578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769224-A-C

16484578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769224-A-G

16484578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769224-A-T

16484597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769243-T-A

16484597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769243-T-C

16484597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769243-T-G

http://identifiers.org/hco/1/GRCh38#16484603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769249-C-A

16484736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769376-G-A

16484736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769376-G-T

16484738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769378-T-C

16484738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769378-T-G

16484740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769380-A-G

16484777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769425-G-A

16484777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769425-G-C

16484777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769425-G-T

16484812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769447-T-C

16484868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769508-T-A

16484868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769508-T-C

16484913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769578-T-C

16484914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769579-G-A

16484914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769579-G-T

16484935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769624-G-T

16485056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769834-G-A

16485056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769834-G-T

16485121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769898-T-C

16485121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769898-T-G

16485132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769909-C-G

16485166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769930-G-A

16485168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769932-G-A

16485386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770081-G-A

16485443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770139-G-A

16485443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770139-G-C

16485443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770139-G-T

16485445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770141-G-A

16485448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770144-G-A

16485448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770144-G-T

16485461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770156-A-G

16485464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770159-G-A

16485464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770159-G-T

http://identifiers.org/hco/1/GRCh38#16485490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770185-C-A

16485490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770185-C-T

16485599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140770262-G-A

16485599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140770262-G-T

16485674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770335-G-A

16485674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770335-G-T

16485675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770336-G-A

16485675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770336-G-C

16485675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770336-G-T

http://identifiers.org/hco/1/GRCh38#16485704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770366-C-A

16485704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770366-C-T

http://identifiers.org/hco/1/GRCh38#16485727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770394-C-A

16485727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770394-C-G

16485727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770394-C-T

http://identifiers.org/hco/1/GRCh38#16485748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770415-C-A

16485748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770415-C-T

http://identifiers.org/hco/1/GRCh38#16485815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770471-C-A

16485815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770471-C-T

16485818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770474-T-A

16486434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770727-G-A

16486434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770727-G-C

16486434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770727-G-T

http://identifiers.org/hco/1/GRCh38#16486470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770763-C-A

16486470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770763-C-G

16486470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770763-C-T

http://identifiers.org/hco/1/GRCh38#16486494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770787-C-A

16486494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770787-C-G

16486494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770787-C-T

16486546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770839-T-G

16486560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770853-G-A

16486560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770853-G-T

16486635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770928-C-G

16486635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770928-C-T

16486658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770951-G-A

16486658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770951-G-C

16486658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140770951-G-T

16486686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770978-G-A

16486686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770978-G-C

16486686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770978-G-T

16486693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770988-T-A

16486695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770990-G-A

16486695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770990-G-C

16486695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770990-G-T

http://identifiers.org/hco/1/GRCh38#16486722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140771016-C-A

16489069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140772773-G-A

http://identifiers.org/hco/1/GRCh38#16489130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140772818-C-A

16489209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140772913-T-C

16489593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773210-G-A

16489593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773210-G-T

16489666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773235-A-G

16489666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773235-A-T

16489708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140773275-G-A

16489708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140773275-G-C

16489708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140773275-G-T

http://identifiers.org/hco/1/GRCh38#16489782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140773349-C-A

16489782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140773349-C-T

http://identifiers.org/hco/1/GRCh38#16489808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140773374-C-A

16489808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773374-C-T

http://identifiers.org/hco/1/GRCh38#16490532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140773648-C-A

16490532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773648-C-T

16490539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773655-T-C

http://identifiers.org/hco/1/GRCh38#16490572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140773682-C-A

16490572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773682-C-G

16490572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773682-C-T

16490720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140773805-G-A

16490720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: non coding transcript exon variant
orthologous variants: 140773805-G-T

http://identifiers.org/hco/1/GRCh38#16490846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140773932-C-A

16490846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140773932-C-T

16490857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140773939-G-C

16490857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140773939-G-T

16490954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140774025-G-T

16490958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140774027-G-A

16490958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140774027-G-C

16490958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140774027-G-T

16490959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140774028-G-C

16490959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140774028-G-T

16491037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774110-G-A

16491037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774110-G-C

16491037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774110-G-T

http://identifiers.org/hco/1/GRCh38#16491085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774158-C-A

16491085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 140774158-C-G

16491085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 140774158-C-T

16491091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140774164-A-G

16491091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140774164-A-T

16491107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774180-G-T

16491135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774209-A-G

http://identifiers.org/hco/1/GRCh38#16491268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774335-C-A

16491268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774335-C-G

16491268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774335-C-T

16491292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774359-G-A

16491292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774359-G-T

http://identifiers.org/hco/1/GRCh38#16491295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774362-A-C

16491295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140774362-A-G

16491798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140782080-A-G

16491799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140782079-G-A

16491799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140782079-G-C

16491802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140782076-T-C

16493974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140781912-C-T

http://identifiers.org/hco/1/GRCh38#16494139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140782076-C-A

16494139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140782076-C-T

16494149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140782086-C-T

16494193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140782132-G-A

16495711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785409-G-C

16495834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785527-G-A

16495857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785547-T-C

16495859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785552-C-T

16495920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785601-C-G

16495921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785606-C-T

16495960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785649-T-C

http://identifiers.org/hco/1/GRCh38#16495970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140785658-C-A

16496092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785743-C-T

16496108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785759-C-G

16496119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785770-G-A

16496122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785773-A-G

16496264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785899-A-G

16496361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785937-C-G

http://identifiers.org/hco/1/GRCh38#16496365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140785941-A-C

http://identifiers.org/hco/1/GRCh38#16496387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140785962-C-A

16496387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785962-C-T

16496411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785982-G-A

16496411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140785982-G-C

16496891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140786086-G-A

16496909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140786104-C-G

16497042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140786249-C-T