16691413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152208401-G-A

16691592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152208548-T-C

16691648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152208595-C-T

16691667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152208614-G-A

http://identifiers.org/hco/1/GRCh38#16691830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152208764-A-C

16691991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152208905-G-A

16692076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152208953-C-T

http://identifiers.org/hco/1/GRCh38#16692088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152208965-C-A

16692128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209002-G-A

16692182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209048-T-G

16692212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209076-C-T

16692621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209568-C-G

16692786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209733-T-C

16692864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209811-C-T

16692884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209831-G-A

16692946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209892-C-T

http://identifiers.org/hco/1/GRCh38#16692967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152209926-C-A

16692967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152209926-C-T

16693056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152210015-C-T

16693399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152210360-G-A

16693428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152210389-C-T

16693454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152210415-G-A

16693454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152210415-G-C

16693454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152210415-G-T

16694053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211002-G-T

16694361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211301-G-T

16694418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211358-C-T

16694544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211505-T-C

16694632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211547-C-T

16694637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211552-G-C

16694704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211585-T-C

16694754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211617-T-A

16694754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211617-T-C

16694804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211651-C-G

16694804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211651-C-T

16694984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152211740-C-T

http://identifiers.org/hco/1/GRCh38#16694999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152211760-C-A

http://identifiers.org/hco/1/GRCh38#16696446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152212541-C-A

16696446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212541-C-T

http://identifiers.org/hco/1/GRCh38#16696590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152212685-C-A

16696590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212685-C-G

16696590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212685-C-T

16696622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212717-A-T

http://identifiers.org/hco/1/GRCh38#16696635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152212730-C-A

16696635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212730-C-T

16696649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212744-G-A

16696649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212744-G-C

16696649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212744-G-T

http://identifiers.org/hco/1/GRCh38#16696652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152212747-C-A

16696652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152212747-C-G

16696946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213028-G-A

16696952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213034-G-A

16696952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213034-G-T

16697019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213093-A-T

16697091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213168-G-A

16697539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213620-G-A

http://identifiers.org/hco/1/GRCh38#16697642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152213721-A-C

16697673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213738-C-T

16697691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213770-T-G

16697865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152213907-T-A

16698219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152214234-C-G

16698219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152214234-C-T

16698291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152214301-A-G

16698291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152214301-A-T

16698319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152214329-C-T

http://identifiers.org/hco/1/GRCh38#16698361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152214355-C-A

16698390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152214375-T-G

16698939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152214867-G-A

16699213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215026-C-G

16699291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215098-C-G

16699291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215098-C-T

16699305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215109-G-A

16699306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215110-G-A

16699306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215110-G-T

16699314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215116-T-C

16699314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215116-T-G

http://identifiers.org/hco/1/GRCh38#16699378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215179-C-A

16699378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215179-C-G

16699378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215179-C-T

16699457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215257-G-A

16699457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215257-G-C

16699457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215257-G-T

16699472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215272-G-A

16699472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215272-G-C

16699472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215272-G-T

http://identifiers.org/hco/1/GRCh38#16699541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215341-C-A

16699541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215341-C-G

16699541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215341-C-T

16699548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215348-G-A

16699548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215348-G-C

16699548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215348-G-T

16699595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215389-A-G

16699595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152215389-A-T

http://identifiers.org/hco/1/GRCh38#16699807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215457-C-A

16699807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215457-C-G

16699807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215457-C-T

http://identifiers.org/hco/1/GRCh38#16699810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215460-C-A

16699810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215460-C-T

16699894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 152215544-G-T

http://identifiers.org/hco/1/GRCh38#16700071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215794-C-A

16700071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215794-C-T

http://identifiers.org/hco/1/GRCh38#16700090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215812-A-C

16700090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152215812-A-G

http://identifiers.org/hco/1/GRCh38#16700121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215841-C-A

16700121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152215841-C-T

16700150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152215871-C-T

16700368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152216076-T-G

http://identifiers.org/hco/1/GRCh38#16700383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152216091-A-C

16700622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 152216327-C-G

16700841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152216517-C-T

16700868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152216561-G-A

16701437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152217121-G-T

16701545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152217177-C-T

16701568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152217200-C-G

16701568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152217200-C-T

16701600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152217237-G-A

16702079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152217903-A-T

16702083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152217934-A-G

16702193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218033-G-A

16702193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218033-G-C

16702193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218033-G-T

16702243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218169-T-C

16702275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218204-C-T

16702279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218208-T-C

16702453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218373-C-G

16702557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218475-G-A

16702557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218475-G-C

16702557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218475-G-T

16702608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218525-G-A

16702690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218603-G-A

16702690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218603-G-C

16702722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218636-C-G

16702870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218796-G-A

16702870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218796-G-T

16702874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218800-G-A

16702874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218800-G-C

16702874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218800-G-T

16702947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 152218873-G-A

16702947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 152218873-G-T

16702981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218915-G-A

16702981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218915-G-T

16703010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218939-G-A

16703010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218939-G-T

http://identifiers.org/hco/1/GRCh38#16703024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152218948-C-A

16703024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218948-C-G

16703024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152218948-C-T

http://identifiers.org/hco/1/GRCh38#16703179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219052-A-C

16703179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219052-A-G

16703179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219052-A-T

16703215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219089-C-T

16703315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219176-C-T

http://identifiers.org/hco/1/GRCh38#16703410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219265-C-A

16703471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219468-C-T

16703492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219493-G-C

16703591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219647-A-G

16703594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219650-A-G

16703742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219789-T-C

16703742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219789-T-G

16703813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219830-G-A

16703813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219830-G-T

http://identifiers.org/hco/1/GRCh38#16703868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219860-A-C

16703868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152219860-A-G

http://identifiers.org/hco/1/GRCh38#16703922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219911-C-A

16703922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219911-C-T

16703932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219919-G-A

16703932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219919-G-T

http://identifiers.org/hco/1/GRCh38#16703936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219923-C-A

16703936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 152219923-C-T

http://identifiers.org/hco/1/GRCh38#16703945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219932-C-A

16703945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 152219932-C-T

16704004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219991-G-C

16704004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219991-G-T

16704007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219994-G-A

16704007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219994-G-T

16704013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152220000-G-T

16704049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220036-C-G

16704049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220036-C-T

16704076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152220063-G-T

16704126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220113-G-A

16704126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220113-G-T

16704168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220155-T-C

16704168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220155-T-G

16704218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220211-T-A

16704218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220211-T-C

http://identifiers.org/hco/1/GRCh38#16704255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152220243-C-A

16704255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152220243-C-T

http://identifiers.org/hco/1/GRCh38#16704370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152220336-C-A

16704370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220336-C-G

16704372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220338-T-C

http://identifiers.org/hco/1/GRCh38#16704398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152220356-A-C

16704401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220359-G-A

16704407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220365-C-T

16704474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220457-A-G

16704480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220467-A-G

16704500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220499-C-T

16704513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220512-C-T

16704516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220515-C-T

http://identifiers.org/hco/1/GRCh38#16704582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152220565-A-C

16704707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220668-T-A

16704708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220669-G-A

16704708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220669-G-C

16704750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220709-G-C

16704791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152220749-G-T

http://identifiers.org/hco/1/GRCh38#16705134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152221110-C-A

16705273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152221233-C-T

16705292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152221250-C-T

16706681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152221810-C-G

16706784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152221915-T-G

16707177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152222775-T-C

http://identifiers.org/hco/1/GRCh38#16707191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152222789-C-A

http://identifiers.org/hco/1/GRCh38#16707227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152222823-C-A

16707227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152222823-C-T

http://identifiers.org/hco/1/GRCh38#16707272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152222871-A-C

16707272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152222871-A-G

16707347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152222946-G-A

16707347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152222946-G-T

16707381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152222980-T-C

16707408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223007-G-A

16707408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223007-G-T

16707432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152223031-G-A

16707432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152223031-G-C

16707432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152223031-G-T

16707481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152223078-A-G

16707532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152223180-G-A

16707532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152223180-G-C

16707532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152223180-G-T

http://identifiers.org/hco/1/GRCh38#16707584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223232-C-A

16707584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223232-C-G

16707584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223232-C-T

16707622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223270-G-A

16707622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223270-G-C

16707622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223270-G-T

16707744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223391-G-A

16707744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223391-G-C

16707744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223391-G-T

16707746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223393-G-A

16707746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223393-G-C

16707746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223393-G-T

http://identifiers.org/hco/1/GRCh38#16707784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223429-C-A

16707784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223429-C-G

16707784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223429-C-T

16707788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223433-G-A

16707788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223433-G-C

16707788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223433-G-T

16707814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223446-A-G

16707814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223446-A-T

16707903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223507-T-A

http://identifiers.org/hco/1/GRCh38#16707928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223532-C-A

16707928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223532-C-G

16707928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223532-C-T

http://identifiers.org/hco/1/GRCh38#16708003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223607-C-A

16708003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223607-C-G

16708003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152223607-C-T

http://identifiers.org/hco/1/GRCh38#16708082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223686-C-A

16708082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 152223686-C-T

http://identifiers.org/hco/1/GRCh38#16708153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223753-C-A

16708153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223753-C-T

16708189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223790-G-A

16708189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223790-G-T

16708277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223853-G-A

16708342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223910-A-T

16708483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152224031-C-T

16709824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152224969-G-A

16709840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152224985-T-C

16709911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225075-G-A

16709934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225100-C-T

16709973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152225139-C-T

16710019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152225153-G-A

16710019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152225153-G-T

16710102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225220-A-G

16710271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152225392-G-A

16710316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225426-T-C

16710358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225448-T-A

16710358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225448-T-C

http://identifiers.org/hco/1/GRCh38#16710365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152225455-C-A

16710365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225455-C-T

16710408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225507-T-C

16710526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152225601-G-A

16710606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152226052-A-G

http://identifiers.org/hco/1/GRCh38#16710721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152226157-C-A

16710721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152226157-C-T

16710754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152226208-A-G

16710772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152226226-C-T

16710902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152226362-C-T

http://identifiers.org/hco/1/GRCh38#16711170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152226563-A-C

16717560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152230568-G-A

16717882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152230883-G-A

16717882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152230883-G-T

16718008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152230981-C-G

16718072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152231045-G-A

16718085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231058-G-C

16718098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231071-C-T

16718235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231194-T-C

16718242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231201-T-A

16718253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231212-G-A

16718253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231212-G-C

16718253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231212-G-T

16718390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231345-G-A

16718442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231395-G-A

16718448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231405-C-T

16718563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231515-G-A

16718601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231553-G-A

16718770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231680-C-T

16718871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231778-C-T

16719042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231917-C-T

16719127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152231973-T-C

16719195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232031-G-A

16719242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232078-C-G

16719242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232078-C-T

16719258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232094-C-T

16719265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232101-G-T

16719302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232133-T-C

16719640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232559-C-G

16719640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232559-C-T

16719645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232588-G-A

16719645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232588-G-T

16719646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232589-G-T

16719687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152232660-G-A

16719980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233332-C-G

16719980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233332-C-T

16719981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233333-G-A

16719981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233333-G-C

16719981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233333-G-T

16719997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233349-G-A

16719999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233351-G-A

16719999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233351-G-T

16720002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233354-G-A

16720002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233354-G-C

16720002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233354-G-T

http://identifiers.org/hco/1/GRCh38#16720070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152233422-C-A

16720070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233422-C-G

16720070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233422-C-T

16720098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23285
most severe consequence: non coding transcript exon variant
orthologous variants: 152233450-C-T