149446969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746500-G-A

149446969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746500-G-C

149446969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746500-G-T

http://identifiers.org/hco/6/GRCh38#149446998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7746465-C-A

149447156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746338-T-C

149447158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746336-G-A

149447158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746336-G-T

149447288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746295-G-T

149447291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746292-T-A

149447291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746292-T-C

149447291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746292-T-G

149447292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746291-G-A

149447292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746291-G-T

149447500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7746231-A-G

149447705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7746078-T-A

149447915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745852-G-T

149447945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745836-A-G

149448583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745423-T-C

149448598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745408-T-C

149448629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745377-T-C

149448694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745316-A-T

149448772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745239-G-A

149448772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745239-G-T

http://identifiers.org/hco/6/GRCh38#149448827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7745193-C-A

149449020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7745016-A-G

149449038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7744998-G-T

149449041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7744995-A-G

149449052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7744984-G-A

149449094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7744942-G-T

149449150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7744884-T-A

149449150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7744884-T-C

http://identifiers.org/hco/6/GRCh38#149449153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744881-C-A

http://identifiers.org/hco/6/GRCh38#149449917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744573-A-C

149449917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744573-A-G

149449945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744551-G-A

149449945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744551-G-C

149449945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744551-G-T

149449951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744545-G-A

149449951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744545-G-T

149450036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744459-A-G

http://identifiers.org/hco/6/GRCh38#149450109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744399-C-A

149450109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744399-C-T

http://identifiers.org/hco/6/GRCh38#149450163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744343-C-A

149450163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744343-C-T

http://identifiers.org/hco/6/GRCh38#149450238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744265-A-C

149450238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744265-A-T

http://identifiers.org/hco/6/GRCh38#149450440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744075-A-C

149450440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744075-A-G

149450440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744075-A-T

http://identifiers.org/hco/6/GRCh38#149450451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744064-C-A

http://identifiers.org/hco/6/GRCh38#149450522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7744001-C-A

149450522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7744001-C-T

149450548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7743970-A-T

149450627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7743892-C-T

149450665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3 prime UTR variant
orthologous variants: 7743851-C-T

149450737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743780-G-A

149450737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743780-G-T

149450791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743726-G-T

http://identifiers.org/hco/6/GRCh38#149450892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7743634-C-A

http://identifiers.org/hco/6/GRCh38#149450924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7743602-C-A

149450924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743602-C-T

149451015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743511-G-A

149451015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743511-G-C

149451015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743511-G-T

http://identifiers.org/hco/6/GRCh38#149451031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7743495-C-A

149451031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743495-C-T

http://identifiers.org/hco/6/GRCh38#149451067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7743459-C-A

149451067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743459-C-G

149451067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743459-C-T

149451071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743455-G-A

149451071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743455-G-T

149451072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743454-A-G

http://identifiers.org/hco/6/GRCh38#149451103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7743423-C-A

149451103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743423-C-G

149451103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743423-C-T

149451111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743415-G-A

149451111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743415-G-T

149451135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743377-A-G

149451158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743362-G-A

149451158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743362-G-T

149451174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743340-G-A

149451174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743340-G-C

149451174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743340-G-T

149451264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743241-C-G

149451316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743189-T-C

149451319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743186-T-A

149451319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743186-T-C

http://identifiers.org/hco/6/GRCh38#149451321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7743184-C-A

149451321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743184-C-T

http://identifiers.org/hco/6/GRCh38#149451326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7743179-C-A

149451326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743179-C-T

149451334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous variant
orthologous variants: 7743171-G-A

149451369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743136-C-T

149451407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743098-A-G

149451419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743086-G-A

149451419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743086-G-T

149451425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7743080-T-C

149451487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7743018-G-T

149451493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743013-G-A

149451493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743013-G-T

149451500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743006-G-A

149451501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743005-A-G

149451503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743003-G-A

149451503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743003-G-T

149451504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743002-G-A

149451504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7743002-G-T

149451520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742987-G-A

149451520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742987-G-C

149451520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742987-G-T

149451536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742971-G-A

149451536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742971-G-T

149451566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742949-G-A

149451566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742949-G-T

http://identifiers.org/hco/6/GRCh38#149451616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7742923-C-A

149451618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742921-G-C

149451618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742921-G-T

149451774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742843-A-T

149451871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742757-G-A

149451900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742739-G-A

149452011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7742648-A-G

http://identifiers.org/hco/6/GRCh38#149452154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7742490-C-A

149452164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742481-A-G

149452227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742447-G-T

149452258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742413-G-A

149452258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742413-G-T

149452282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742389-G-T

149452310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742361-G-T

149452365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742330-T-C

149452367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742328-T-A

http://identifiers.org/hco/6/GRCh38#149452394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7742299-C-A

149452428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742249-C-T

http://identifiers.org/hco/6/GRCh38#149452431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7742246-C-A

149452431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742246-C-T

http://identifiers.org/hco/6/GRCh38#149452432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7742245-C-A

149452432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742245-C-T

http://identifiers.org/hco/6/GRCh38#149452450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7742227-A-C

149452450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742227-A-G

149452478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742208-A-G

149452478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742208-A-T

149452493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 7742195-A-G

149452673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7742039-T-C

149452673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7742039-T-G

149452740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7741970-G-A

149452740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7741970-G-T

149452741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7741969-G-A

149452741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7741969-G-T

149454298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740386-T-A

149454401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740295-G-C

149454464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740241-C-G

149454605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740092-T-C

149454632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740065-G-C

149454654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740043-C-T

149454655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740042-G-A

149454678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7740022-C-T

149454786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7739912-T-C

149454786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7739912-T-G

149454862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7739833-A-G

http://identifiers.org/hco/6/GRCh38#149454863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7739832-C-A

149454917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7739749-G-A

149455218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7739539-A-G

149455273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7739468-C-G

149456720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7738328-T-G

149456729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7738319-T-C

149456771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7738277-C-G

149456786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense variant
orthologous variants: 7738262-G-A

http://identifiers.org/hco/6/GRCh38#149456851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7738197-C-A

149456851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: synonymous_variant, undefined
orthologous variants: 7738197-C-T

http://identifiers.org/hco/6/GRCh38#149456879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7738169-A-C

149456935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, undefined
orthologous variants: 7738115-C-T

149456971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7738087-A-G

149458809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7737436-T-G

149458846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7737397-A-G

http://identifiers.org/hco/6/GRCh38#149458925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7737328-A-C

149459029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7737169-G-A

149459076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7737058-G-T

149459100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7737029-T-C

149459111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7737018-A-T

149459361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7736765-A-T

149459379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7736746-A-G

149459478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7736656-C-G

149459478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7736656-C-T

149459709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7736585-G-A

149459731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7736565-T-C

149461352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729499-A-G

149461477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729398-A-G

149461479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729396-T-C

149461481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729394-G-C

149461566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729272-A-G

149461654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729206-G-A

149461654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729206-G-T

http://identifiers.org/hco/6/GRCh38#149461660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7729200-A-C

149461660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729200-A-G

149461660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7729200-A-T

149461684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7729184-A-G

149461982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7728939-A-G

149462002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7728918-C-T

149462008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7728912-A-G

149462028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7728909-T-C

http://identifiers.org/hco/6/GRCh38#149463143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7728654-A-C

http://identifiers.org/hco/6/GRCh38#149463149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7728648-A-C

149463168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7728629-A-G

149463308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7728493-T-C

149463778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7727934-A-T

149466574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7724305-A-G

149468435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7722938-C-T

149468573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7722815-C-T

149468605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7722782-A-G

149468613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7722774-C-T

149469750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7722064-G-A

149469874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7721913-G-A

149469884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7721903-C-T

149470129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7721547-T-C

149470157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7721514-A-G

149471445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7720504-G-A

149471683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7720317-G-A

149471734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7720178-T-C

149471755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7720127-C-T

149471890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7719956-C-T

149472075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7719587-G-A

149472541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7719133-G-A

149472542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7719132-A-G

149472542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7719132-A-T

149472612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7719051-T-C

149472754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7718893-T-C

149473054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7718039-C-T

149473135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717959-A-G

149473163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717931-C-T

149473227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717882-G-C

149473265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717844-A-G

149473572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717575-T-C

http://identifiers.org/hco/6/GRCh38#149473617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7717530-C-A

149473617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717530-C-T

149473920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717252-G-T

http://identifiers.org/hco/6/GRCh38#149473924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7717248-C-A

149473929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7717243-T-C

149474296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7715853-C-G

149474528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7715612-T-G

149474618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7715522-A-G

149474682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7715454-G-T

http://identifiers.org/hco/6/GRCh38#149474693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7715439-C-A

149474693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7715439-C-T

http://identifiers.org/hco/6/GRCh38#149474696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7715436-C-A

149474698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7715434-G-A

149474698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7715434-G-T

149474830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7715297-C-T

149478880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7713759-C-T

149480907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7711575-C-T

http://identifiers.org/hco/6/GRCh38#149481121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7711388-A-C

149481738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710984-G-A

http://identifiers.org/hco/6/GRCh38#149481815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7710923-C-A

149481815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710923-C-T

149481890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7710818-G-A

149481915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710793-G-A

149481915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710793-G-T

149482148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710556-C-T

149482231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7710464-C-T

149482313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710407-T-A

149482313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710407-T-C

149482364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710358-T-C

149482485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710236-A-G

149482605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710152-A-G

149482634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710123-G-T

http://identifiers.org/hco/6/GRCh38#149482645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7710110-C-A

149482655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710098-G-C

149482657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710096-T-C

149482677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710076-G-A

149482725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710014-C-T

149482726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7710013-G-A

149482801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7709911-T-C

149482851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7709862-T-C

149482901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7709824-G-A

149482901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7709824-G-T

http://identifiers.org/hco/6/GRCh38#149483090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7709726-C-A

149483090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7709726-C-T

149483115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7709701-G-A

149483115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7709701-G-T

149483276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7709508-T-C

http://identifiers.org/hco/6/GRCh38#149483310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7709477-A-C

149483324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7709448-G-T

http://identifiers.org/hco/6/GRCh38#149483558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7709252-C-A

http://identifiers.org/hco/6/GRCh38#149483629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7709183-A-C

149483629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7709183-A-G

http://identifiers.org/hco/6/GRCh38#149484588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7708520-C-A

149484768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7708368-G-A

149484768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron variant
orthologous variants: 7708368-G-T

149484785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, undefined
orthologous variants: 7708351-G-A

149484785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: intron_variant, undefined
orthologous variants: 7708351-G-T

http://identifiers.org/hco/6/GRCh38#149484862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7708276-C-A

149484862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 7708276-C-T

149484933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 7708194-G-A

149484933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 7708194-G-T

149484936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 7708191-G-T

149484992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21175
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 7708137-G-A