98868539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440841-G-A

98868539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440841-G-T

98868572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440813-A-G

98868625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440769-T-C

98868641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440750-C-T

98868706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440681-T-C

98868719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440671-C-T

98868809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440587-T-C

98868841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440555-C-T

98868964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440434-G-A

98869118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440307-A-G

98869229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22440238-G-A

98870092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22438142-C-T

98870177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22438064-A-G

98870243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437986-G-T

http://identifiers.org/hco/6/GRCh38#98870270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22437954-C-A

98870281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437943-T-C

98870473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437800-A-G

98870483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437790-C-G

98870483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437790-C-T

98870651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437607-T-A

98870651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437607-T-C

http://identifiers.org/hco/6/GRCh38#98870657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22437601-C-A

98870657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437601-C-T

http://identifiers.org/hco/6/GRCh38#98870728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22437535-C-A

98870763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437500-A-G

http://identifiers.org/hco/6/GRCh38#98871168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22437302-C-A

98871168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437302-C-T

http://identifiers.org/hco/6/GRCh38#98871226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22437244-C-A

98871333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437138-G-A

98871440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22437052-G-T

98871504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436989-C-G

98871504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436989-C-T

98871514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436979-T-C

http://identifiers.org/hco/6/GRCh38#98871523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22436970-C-A

98871523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436970-C-G

98871523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436970-C-T

98871672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436847-T-C

98871682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436837-A-G

http://identifiers.org/hco/6/GRCh38#98871732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22436787-C-A

98871834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436715-G-A

98871834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436715-G-C

98871863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22436687-T-C

http://identifiers.org/hco/6/GRCh38#98871906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22436646-C-A

http://identifiers.org/hco/6/GRCh38#98872186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22436416-A-C

http://identifiers.org/hco/6/GRCh38#98872223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22436380-C-A

http://identifiers.org/hco/6/GRCh38#98872338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22436250-A-C

http://identifiers.org/hco/6/GRCh38#98872664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22435884-C-A

98872704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22435850-C-G

98872719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22435835-A-G

98872802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22435773-G-A

98872802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22435773-G-T

98872814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22435761-G-T

http://identifiers.org/hco/6/GRCh38#98872850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22435734-C-A

98872954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22435631-G-A

http://identifiers.org/hco/6/GRCh38#98873442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22434567-A-C

98873549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434466-C-T

98873568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434448-G-C

98873598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434378-A-G

98873598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434378-A-T

98873599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434377-G-T

98873608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434368-T-C

98873614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434362-G-A

98873614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22434362-G-T

http://identifiers.org/hco/6/GRCh38#98873826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22434169-C-A

http://identifiers.org/hco/6/GRCh38#98874066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22433933-C-A

98874066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22433933-C-T

98874254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22433752-T-G

98874270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22433736-A-T

http://identifiers.org/hco/6/GRCh38#98875030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22430782-A-C

http://identifiers.org/hco/6/GRCh38#98875121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22430694-A-C

98875121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430694-A-T

http://identifiers.org/hco/6/GRCh38#98875128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22430687-C-A

98875128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430687-C-T

98875132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430683-T-A

98875132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430683-T-C

98875132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430683-T-G

98875133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430682-G-A

98875133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430682-G-T

98875238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430567-A-G

98875447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22427428-T-C

98875524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22427351-C-G

98875733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22427142-A-T

98875764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22427112-G-T

http://identifiers.org/hco/6/GRCh38#98875809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22427074-A-C

http://identifiers.org/hco/6/GRCh38#98875847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22427038-C-A

98875856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22427029-A-G

98875918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22426954-T-C

98876136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22426450-C-T

http://identifiers.org/hco/6/GRCh38#98876333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22426253-A-C

98878700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22424003-T-C

98878891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423823-A-G

98878965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423750-A-G

http://identifiers.org/hco/6/GRCh38#98879340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22423466-A-C

98879536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423299-A-T

98880072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423148-T-C

98880082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423138-T-C

98880243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422991-A-G

http://identifiers.org/hco/6/GRCh38#98880404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22422907-A-C

98880415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422896-G-C

98880415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422896-G-T

98880455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422879-G-A

98880455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422879-G-C

98880455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422879-G-T

98880461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422873-G-A

98880461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422873-G-C

98880461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422873-G-T

98880475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422859-G-A

98880475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422859-G-T

98880499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422836-G-T

98880671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422668-A-G

98881050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422283-T-C

98881651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421311-G-T

98881668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421293-T-C

98881672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421289-A-T

98881749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421218-A-G

98881807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421161-C-G

98881862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421106-T-C

98881873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421100-T-G

98881922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421050-C-T

98881941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421020-T-C

98881953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421011-C-T

98886672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419486-G-C

98887190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419043-C-T

98887380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418948-G-C

98887814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417440-T-C

http://identifiers.org/hco/6/GRCh38#98888023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22417248-C-A

98888023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417248-C-T

98888149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417154-T-A

98888171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417132-G-A

98888183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417120-T-A

98888265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417053-T-G

98888439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22416688-T-A

http://identifiers.org/hco/6/GRCh38#98888810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22411571-A-C

98888879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22411507-C-T

98888926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22411467-C-T

98889107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22411330-G-A

98892256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22409163-T-C

98892370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22409075-G-C

98893101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22408397-T-C

http://identifiers.org/hco/6/GRCh38#98895494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22408225-C-A

98895786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22407954-T-G

98895862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22407882-G-A

98895887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22407859-A-G

98899551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403460-A-G

98899563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403448-T-A

98899563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403448-T-C

98899743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403267-G-C

98899751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403259-A-T

98899856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403186-T-C

98900954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398847-G-T

98900959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398842-C-T

98901155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398662-G-A

98901370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398486-G-A

98901882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22394720-T-C

http://identifiers.org/hco/6/GRCh38#98902570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22393786-C-A

98902668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393719-C-T

98902669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393718-A-T

98902751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393639-A-G

98903442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22393003-G-A

98903471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22392974-C-T

98903508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22392944-T-C

98903656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22392806-A-G

98903716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22392748-G-A

98903716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22392748-G-C

98903757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22392707-C-T

98904185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22392150-T-A

98905241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391063-G-A

98905252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391057-C-T

98905364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390973-T-C

http://identifiers.org/hco/6/GRCh38#98905453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22390892-C-A

98905453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22390892-C-G

98905473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22390872-T-A

98905473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22390872-T-C

98905558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22390787-T-C

98905600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22390745-A-G

98905648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22390697-T-C

98905726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390620-G-T

98905750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390570-G-A

98905750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390570-G-T

98907483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390032-A-G

98907534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22389985-T-C

98907629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22389890-G-T

98907731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22389780-C-T

98908642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388098-T-A

98909039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387637-A-T

http://identifiers.org/hco/6/GRCh38#98909194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22387466-A-C

98909203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387448-C-G

98909243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387408-T-C

98909274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387382-A-G

98909318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387341-C-G

98909392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387277-C-T

98909899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386809-G-A

98909954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386755-T-C

98910201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386521-G-C

98910210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386515-G-A

98910210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386515-G-T

98910314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386410-G-A

98910314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386410-G-C

98917318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386301-A-G

98917318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386301-A-T

98917456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386168-A-G

98917510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386114-A-G

98917534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386090-A-G

98917539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386085-C-G

98917539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 22386085-C-T

http://identifiers.org/hco/6/GRCh38#98917552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22386072-C-A

98917579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386045-G-C

98917597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386027-G-A

98917597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386027-G-C

98917597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386027-G-T

98917603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386021-T-A

98917603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22386021-T-C

98917687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22385937-T-G

98917803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385832-G-A

98917803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385832-G-T

98917846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385785-A-G

98919034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381995-G-A

98919098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381939-T-C

98919232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381213-C-T

98921736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380833-C-T

98921806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380767-T-A

98922164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380604-T-C

98922223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380601-G-C

98922467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380360-A-T

98922908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380140-T-C

98923123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22379954-C-T

98923336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22379825-G-C

98923345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22379817-C-T

98924776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378731-C-T

98924932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378559-T-G

98925021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378476-C-T

98925022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378475-G-A

98925230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378284-A-T

98925419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378167-A-G

98925999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22377594-C-T

98926445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22377114-T-A

98926982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22376570-G-A

98927028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22376524-T-A

98927398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376131-A-T

98927750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22375723-G-T

98928087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375361-C-T

98928219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22368895-T-A

98928946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22368496-T-A

98929052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22368393-T-C

98929152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22368293-A-T

98929216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22368227-G-A

http://identifiers.org/hco/6/GRCh38#98929619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22368167-A-C

98929912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22367918-C-G

98930147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22367713-A-G

98930148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22367712-T-C

98931280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22367376-A-T

http://identifiers.org/hco/6/GRCh38#98931495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22367162-A-C

98932300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22366261-T-C

98932531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22366027-T-C

98932596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22365963-G-A

98932822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22365782-C-G

98932853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22365752-T-C

98932916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22365704-A-G

98933420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22365234-G-A

98934097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364647-T-G

98934224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364520-C-G

98934224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364520-C-T

98934282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364466-C-T

98934297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364451-A-G

98934304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364443-G-A

98935035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22363158-A-T

98935066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22363125-A-G

98935182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22363012-A-G

98935198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22362996-T-A

http://identifiers.org/hco/6/GRCh38#98935281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22362928-C-A

98935281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22362928-C-T

98935413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22362825-G-A

98936108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22361780-A-G

98945241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22359766-T-C

98945607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22359515-A-G

98945610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22359512-G-A

98945812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22359346-A-G

98945943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22359230-G-C

98946376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22358699-G-A

98946450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22358630-G-C

98946787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22358338-A-G

98946843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22358290-G-A

98947531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22357870-G-A

98947531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22357870-G-C

98947578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22357848-C-G

98947643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22357813-G-C

98947643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22357813-G-T

http://identifiers.org/hco/6/GRCh38#98947684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22357778-C-A

98947684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22357778-C-T

98947883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22357614-C-T

http://identifiers.org/hco/6/GRCh38#98947919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13601
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22357580-C-A