100537153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998113-C-T

100537195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998155-C-T

http://identifiers.org/hco/14/GRCh38#100537288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#108998239-C-A

100537288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998239-C-T

http://identifiers.org/hco/14/GRCh38#100537335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#108998280-A-C

100537371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998322-G-A

100537371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998322-G-T

http://identifiers.org/hco/14/GRCh38#100537381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#108998342-C-A

100537381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998342-C-T

100537540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998493-G-A

100537545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998498-T-C

100537582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998530-G-A

100537582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998530-G-T

http://identifiers.org/hco/14/GRCh38#100537746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#108998686-C-A

100537746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998686-C-G

100537746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998686-C-T

100537811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998769-C-T

100537933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998877-G-A

100537933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108998877-G-T

100537987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108998928-G-A

100537987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 108998928-G-C

100538071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108999012-G-A

http://identifiers.org/hco/14/GRCh38#100538200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#108999138-C-A

100538200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108999138-C-G

100538200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108999138-C-T

100538212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108999150-A-G

100538530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108999495-G-A

http://identifiers.org/hco/14/GRCh38#100538539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#108999504-C-A

100538539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108999504-C-T

100538629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108999594-C-G

100538629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108999594-C-T

100538666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108999631-G-A

100538666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108999631-G-T

100539136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109000098-G-A

100539136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109000098-G-T

100539376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109000335-G-A

100539376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109000335-G-T

100539554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109000485-C-T

100539570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109000500-G-T

100539693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109000577-T-C

100539693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109000577-T-G

100540035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109000899-T-A

100540035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109000899-T-C

100540035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109000899-T-G

100540178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109000987-A-G

100540311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001067-G-A

100540311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001067-G-C

100540411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001165-T-C

100540411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001165-T-G

100540429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001183-T-C

100540596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001354-G-A

100540596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001354-G-C

100540605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001363-C-T

http://identifiers.org/hco/14/GRCh38#100540722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109001444-C-A

100540722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109001444-C-T

100541516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109002054-G-A

100543559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109002692-T-C

100543706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109002791-A-T

http://identifiers.org/hco/14/GRCh38#100543763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109002821-C-A

100543789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109002851-T-C

100543927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109002991-G-A

100543927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109002991-G-C

100543927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109002991-G-T

100543994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003052-C-T

100544064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003111-G-A

100544064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003111-G-C

100544064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003111-G-T

100544078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003125-T-C

100544368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003338-C-T

http://identifiers.org/hco/14/GRCh38#100544848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109003515-C-A

100544848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003515-C-G

100544848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003515-C-T

100544912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003549-T-C

100544931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003563-G-C

100544931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003563-G-T

100544932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003564-T-C

100544933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003565-C-T

http://identifiers.org/hco/14/GRCh38#100544994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109003573-C-A

100544994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003573-C-T

http://identifiers.org/hco/14/GRCh38#100545129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109003726-C-A

100545129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109003726-C-T

100545175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109003765-G-A

100545175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109003765-G-T

100545316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109003868-T-C

100545316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109003868-T-G

http://identifiers.org/hco/14/GRCh38#100545361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109003889-C-A

100545361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003889-C-T

http://identifiers.org/hco/14/GRCh38#100545410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109003906-A-C

100545410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003906-A-G

http://identifiers.org/hco/14/GRCh38#100545412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109003908-C-A

http://identifiers.org/hco/14/GRCh38#100545471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109003955-A-C

100545471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003955-A-G

100545477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003961-T-C

100545482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109003966-C-G

http://identifiers.org/hco/14/GRCh38#100546414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109004690-C-A

100546451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109004729-T-A

100546451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109004729-T-C

http://identifiers.org/hco/14/GRCh38#100546486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109004764-C-A

100546486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109004764-C-T

http://identifiers.org/hco/14/GRCh38#100546498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109004775-C-A

100546578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109004855-G-C

100546578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109004855-G-T

100546587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109004864-G-A

100546587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109004864-G-C

100546587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109004864-G-T

100546595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109004872-G-T

http://identifiers.org/hco/14/GRCh38#100546825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109005090-C-A

100546825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005090-C-T

100547981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109005399-C-T

100547990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109005406-G-A

http://identifiers.org/hco/14/GRCh38#100548003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109005419-C-A

100548003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005419-C-T

100548253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005597-C-T

100548320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005644-G-A

100548320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005644-G-T

100548390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005674-G-A

100548390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005674-G-T

http://identifiers.org/hco/14/GRCh38#100548409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109005693-C-A

100548460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109005738-T-C

100548460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109005738-T-G

http://identifiers.org/hco/14/GRCh38#100548472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#109005750-C-A

100548556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005818-T-C

http://identifiers.org/hco/14/GRCh38#100548557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109005819-C-A

100548693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005955-C-T

100548715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005977-T-C

100548730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005988-G-A

100548730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109005988-G-T

http://identifiers.org/hco/14/GRCh38#100548732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109005990-C-A

100548769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006020-G-T

100548835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006045-A-T

100548837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006047-A-G

100548837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006047-A-T

http://identifiers.org/hco/14/GRCh38#100548870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006079-C-A

100548870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006079-C-T

100548885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006092-G-A

100548885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006092-G-T

http://identifiers.org/hco/14/GRCh38#100548924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006136-C-A

100548924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006136-C-G

100548924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006136-C-T

http://identifiers.org/hco/14/GRCh38#100548944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006151-C-A

100548944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006151-C-T

http://identifiers.org/hco/14/GRCh38#100549067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006265-C-A

http://identifiers.org/hco/14/GRCh38#100549069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006267-C-A

http://identifiers.org/hco/14/GRCh38#100549070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006268-C-A

100549070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006268-C-T

100549160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006317-C-T

http://identifiers.org/hco/14/GRCh38#100549362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006398-C-A

100549362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006398-C-T

http://identifiers.org/hco/14/GRCh38#100549571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006548-C-A

100549571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006548-C-T

http://identifiers.org/hco/14/GRCh38#100549588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006565-C-A

100549679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006644-T-C

http://identifiers.org/hco/14/GRCh38#100549738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006688-C-A

100549738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006688-C-T

100549789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006774-G-A

100549789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006774-G-T

http://identifiers.org/hco/14/GRCh38#100549803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006795-C-A

100549803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006795-C-T

100549820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109006813-T-C

http://identifiers.org/hco/14/GRCh38#100549897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109006917-C-A

100550308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007214-C-T

100550342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007244-T-C

http://identifiers.org/hco/14/GRCh38#100550388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109007290-C-A

100550388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007290-C-T

100550389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007291-A-G

100550389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007291-A-T

100550479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109007394-G-A

100550479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109007394-G-T

100550601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007469-G-A

100550831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007622-C-T

100550926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109007659-C-T

100551343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109008038-A-G

100551581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109008245-A-T

100551746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109008387-G-A

100554263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109009618-T-G

100554380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109009737-C-G

100554489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109009824-C-T

100554565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109009896-G-A

100554877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109010132-T-C

100555445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109010656-C-G

100555582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109010776-G-A

100555586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109010780-T-G

100555621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109010813-G-A

100555999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109010973-G-A

100555999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109010973-G-T

100556179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109011087-T-A

100556179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109011087-T-C

100556339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109011209-C-T

100556582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109011420-A-T

100562031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109013954-A-G

100562078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109013993-T-C

100562189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109014106-T-A

http://identifiers.org/hco/14/GRCh38#100562570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109014217-C-A

100562826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109014438-C-T

100562883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109014498-G-A

100563294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109015012-C-T

http://identifiers.org/hco/14/GRCh38#100563417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109015139-C-A

100564106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109015654-A-G

100564171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109015706-G-A

100564314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109015803-G-A

100564662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016048-T-G

100564745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016129-G-A

100564787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016167-G-A

100565168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016492-G-A

100565168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016492-G-C

100565196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016507-G-T

100565200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016512-G-A

100565601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109016817-T-A

100566781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109017908-G-C

100567690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109018617-G-T

100567761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109018674-A-T

http://identifiers.org/hco/14/GRCh38#100567772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109018685-C-A

http://identifiers.org/hco/14/GRCh38#100567943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109018792-C-A

100567943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109018792-C-G

100567943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109018792-C-T

100568979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: -G-A

100569586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 109020251-G-A

100569586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 109020251-G-T

http://identifiers.org/hco/14/GRCh38#100569639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109020301-C-A

100569639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 109020301-C-T

100569705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 109020368-A-G

http://identifiers.org/hco/14/GRCh38#100569847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109020493-A-C

100569847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109020493-A-G

100569847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109020493-A-T

100569880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109020520-A-G

http://identifiers.org/hco/14/GRCh38#100569920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109020543-C-A

100569930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109020553-T-C

100570000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109020616-G-T

100570303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109020920-T-C

http://identifiers.org/hco/14/GRCh38#100570595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109021182-C-A

100573972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109022988-T-C

100574065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109023064-G-C

100574540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109023420-A-T

100574589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109023471-G-A

100574889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109023675-C-G

100574996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109023803-G-A

100577230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109024694-A-G

100577264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109024720-G-A

100577332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109024763-G-A

100577332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109024763-G-C

100577473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109024859-T-A

100577473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109024859-T-C

100577473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109024859-T-G

http://identifiers.org/hco/14/GRCh38#100577478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109024864-C-A

100577478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: 109024864-C-T

100577479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109024865-T-C

http://identifiers.org/hco/14/GRCh38#100577593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109024979-C-A

100577593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109024979-C-T

http://identifiers.org/hco/14/GRCh38#100577648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109025034-C-A

100577648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: 109025034-C-G

100577648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: 109025034-C-T

100577746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109025132-G-A

100577746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: 109025132-G-T

http://identifiers.org/hco/14/GRCh38#100577804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109025184-C-A

http://identifiers.org/hco/14/GRCh38#100577810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109025190-C-A

http://identifiers.org/hco/14/GRCh38#100577816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109025196-A-C

http://identifiers.org/hco/14/GRCh38#100577837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109025202-C-A

100577869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109025234-G-A

100577869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109025234-G-C

100577869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 109025234-G-T

100577961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109025326-G-A

100578023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109025368-G-A

http://identifiers.org/hco/14/GRCh38#100578100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109025425-A-C

100578100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109025425-A-G

100581467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109030109-C-T

100582695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109030663-C-T

100583258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109031165-A-G

100583275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109031177-C-T

http://identifiers.org/hco/14/GRCh38#100583524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109031428-C-A

100584725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032105-T-C

100585044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032377-C-T

100585049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032382-C-G

100585087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032411-T-A

100585125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032442-T-A

100585135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032453-G-C

http://identifiers.org/hco/14/GRCh38#100585409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109032505-C-A

100585409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032505-C-T

100585463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032531-T-A

100585463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032531-T-C

100585532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032562-G-A

100585710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109032813-T-G

100586210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109033239-A-T

100586562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, undefined
orthologous variants: 109033586-C-T

100586708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron variant
orthologous variants: 109033721-T-C

100587182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, undefined
orthologous variants: 109033990-T-C

100587182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: intron_variant, undefined
orthologous variants: 109033990-T-G

http://identifiers.org/hco/14/GRCh38#100587267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#109034070-C-A

100587267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 109034070-C-G

100587267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24163
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 109034070-C-T