149776083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48425204-G-A

http://identifiers.org/hco/7/GRCh38#149776106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48425226-C-A

149776106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425226-C-T

http://identifiers.org/hco/7/GRCh38#149776134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48425244-C-A

149776134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425244-C-T

149776139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425249-G-A

149776139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425249-G-T

http://identifiers.org/hco/7/GRCh38#149776194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48425296-C-A

149776194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425296-C-T

149776259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48425340-A-G

149776297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48425381-G-T

149776304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48425388-G-T

149776307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48425391-G-A

http://identifiers.org/hco/7/GRCh38#149776332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48425416-C-A

149776444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48425529-G-A

149776444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48425529-G-T

149776497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48425582-T-C

149776551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48425636-G-C

149776551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48425636-G-T

http://identifiers.org/hco/7/GRCh38#149776583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48425671-C-A

149776583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425671-C-T

149776597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425685-G-C

149776597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425685-G-T

149776674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425758-T-A

149776674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425758-T-C

149776749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425831-C-T

149776796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425868-T-G

149776797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425869-G-T

149776818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425887-G-A

149776818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425887-G-C

149776818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425887-G-T

149776861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48425955-C-G

149776904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426009-C-T

149777046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426150-G-A

149777046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426150-G-T

http://identifiers.org/hco/7/GRCh38#149777101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48426212-C-A

149777147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426265-C-G

149777147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426265-C-T

http://identifiers.org/hco/7/GRCh38#149777162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48426280-C-A

149777247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426362-G-A

149777247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426362-G-T

http://identifiers.org/hco/7/GRCh38#149777272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48426387-C-A

149777272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426387-C-T

http://identifiers.org/hco/7/GRCh38#149777284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48426399-C-A

149777284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426399-C-G

149777284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426399-C-T

149777367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426482-G-A

149777367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426482-G-T

149777461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426549-G-A

149777461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426549-G-T

149777472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426560-G-T

149777483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426571-G-A

149777502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426590-G-A

149777506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426594-C-G

149777506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426594-C-T

149777516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426604-T-C

149777526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426614-T-C

http://identifiers.org/hco/7/GRCh38#149777536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48426624-C-A

149777536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426624-C-T

http://identifiers.org/hco/7/GRCh38#149777572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48426657-C-A

149777572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426657-C-G

http://identifiers.org/hco/7/GRCh38#149777605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48426665-C-A

149777605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48426665-C-T

149777670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426730-C-T

149777727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426787-C-T

149777783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48426843-C-T

149777900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426962-G-A

149777900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426962-G-T

149777925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48426987-T-A

149778029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48427088-G-A

149778029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48427088-G-T

http://identifiers.org/hco/7/GRCh38#149778039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48427098-C-A

149778039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48427098-C-T

http://identifiers.org/hco/7/GRCh38#149778103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48427133-C-A

149778109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48427139-A-G

149778773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48427988-G-A

149778773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48427988-G-C

http://identifiers.org/hco/7/GRCh38#149778792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48428007-C-A

149778835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48428050-T-G

149778908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48428123-C-T

http://identifiers.org/hco/7/GRCh38#149778992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48428232-C-A

149778992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48428232-C-T

http://identifiers.org/hco/7/GRCh38#149779005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48428249-A-C

149779015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48428259-C-T

149779060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48428304-A-G

149779462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48428606-G-T

149779463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48428607-G-T

http://identifiers.org/hco/7/GRCh38#149779509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48428646-C-A

149779509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48428646-C-T

http://identifiers.org/hco/7/GRCh38#149779663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48428796-C-A

149779885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48429011-T-C

149780091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429228-G-T

149780241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429400-G-A

149780241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429400-G-T

http://identifiers.org/hco/7/GRCh38#149780257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48429416-C-A

149780257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429416-C-T

149780356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429515-T-C

149780356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429515-T-G

149780398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429557-G-T

http://identifiers.org/hco/7/GRCh38#149780474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48429633-C-A

http://identifiers.org/hco/7/GRCh38#149780531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48429689-C-A

149780531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48429689-C-G

149780531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48429689-C-T

http://identifiers.org/hco/7/GRCh38#149780637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48429767-C-A

149780637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48429767-C-G

149780637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48429767-C-T

149780743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48429832-A-G

149780743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48429832-A-T

http://identifiers.org/hco/7/GRCh38#149780766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48429856-C-A

149780782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429872-G-A

149780782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429872-G-T

149780796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429886-G-A

149780796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429886-G-T

149780812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429902-G-T

149780814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429904-C-G

149780814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429904-C-T

149780815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429905-A-G

149780899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48429989-A-G

149780949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430039-T-C

http://identifiers.org/hco/7/GRCh38#149781029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48430113-A-C

149781305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430253-A-G

149781346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430290-C-T

149781532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430482-T-C

149781665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430580-G-T

149781742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430609-G-A

http://identifiers.org/hco/7/GRCh38#149781848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48430675-A-C

149782042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430800-G-T

http://identifiers.org/hco/7/GRCh38#149782045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48430803-A-C

149782053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430811-T-G

http://identifiers.org/hco/7/GRCh38#149782060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48430818-C-A

149782060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430818-C-T

149782097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430846-G-A

149782097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430846-G-C

149782097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430846-G-T

149782143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430871-G-A

149782143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430871-G-T

149782150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430878-G-A

149782150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430878-G-C

149782150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48430878-G-T

149782186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48430914-A-G

149782209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48430937-C-T

149782271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48430999-G-A

149782271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48430999-G-T

http://identifiers.org/hco/7/GRCh38#149782277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48431005-C-A

149782277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48431005-C-T

149782329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431056-T-A

149782329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431056-T-C

http://identifiers.org/hco/7/GRCh38#149782330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48431057-C-A

149782330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431057-C-G

149782330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431057-C-T

149782398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431145-A-G

149782509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431267-G-T

http://identifiers.org/hco/7/GRCh38#149782724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48431500-C-A

149782724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431500-C-T

http://identifiers.org/hco/7/GRCh38#149782844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48431615-C-A

149783014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48431785-G-T

149783063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431832-G-A

149783063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48431832-G-T

149783112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48431878-G-A

149783112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48431878-G-T

149783160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48431926-A-G

149783291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432054-T-A

149783293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432056-G-A

149783445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432180-T-C

149783467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432201-C-T

149783485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432219-G-C

149783485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432219-G-T

http://identifiers.org/hco/7/GRCh38#149783531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48432264-C-A

149783531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432264-C-G

149783565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432298-G-A

149783565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432298-G-T

149783624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432357-T-C

http://identifiers.org/hco/7/GRCh38#149783718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48432439-C-A

149783718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432439-C-G

149783718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432439-C-T

149783819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432544-G-A

149783819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48432544-G-T

149783965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432666-G-T

149784084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48432785-G-C

149784172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48432873-T-C

149784174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48432875-G-T

149784184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48432894-G-A

149784184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48432894-G-T

149784232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48432965-T-C

http://identifiers.org/hco/7/GRCh38#149784421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48433303-C-A

149784678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48433746-G-T

149784679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48433747-G-T

http://identifiers.org/hco/7/GRCh38#149784708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48433772-C-A

149784708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48433772-C-T

149784712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48433776-G-A

149784740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48433808-A-G

149784813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48433894-C-T

149784932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48434013-C-T

149785064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434145-A-G

http://identifiers.org/hco/7/GRCh38#149785290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48434363-C-A

149785290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434363-C-T

149785313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434384-G-A

149785313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434384-G-C

149785313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434384-G-T

http://identifiers.org/hco/7/GRCh38#149785335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48434405-C-A

149785454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434478-G-T

149785543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48434565-C-T

http://identifiers.org/hco/7/GRCh38#149785550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48434572-C-A

149785550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48434572-C-G

149785550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48434572-C-T

149785571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48434593-T-C

149785650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48434672-G-T

http://identifiers.org/hco/7/GRCh38#149785745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48434767-C-A

149785745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434767-C-T

149785777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434795-G-A

149785777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434795-G-T

149785847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434836-T-A

149785847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434836-T-C

http://identifiers.org/hco/7/GRCh38#149785879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48434866-C-A

149785879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434866-C-T

149785885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434870-A-G

149785942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434911-T-A

149785942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48434911-T-G

149786032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48435001-A-G

149786097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48435048-G-A

149786147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48435098-T-G

http://identifiers.org/hco/7/GRCh38#149786171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435122-C-A

149786171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48435122-C-T

http://identifiers.org/hco/7/GRCh38#149786272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435218-C-A

149786272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435218-C-T

http://identifiers.org/hco/7/GRCh38#149786308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435254-C-A

149786308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435254-C-T

http://identifiers.org/hco/7/GRCh38#149786337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435263-C-A

149786379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435315-G-A

149786379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435315-G-C

149786379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435315-G-T

http://identifiers.org/hco/7/GRCh38#149786454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435363-C-A

149786454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435363-C-T

http://identifiers.org/hco/7/GRCh38#149786459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435368-C-A

149786459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435368-C-G

149786459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435368-C-T

149786474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435386-T-C

http://identifiers.org/hco/7/GRCh38#149786499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435411-C-A

149786499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435411-C-T

149786936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435544-C-T

149786964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435568-T-C

http://identifiers.org/hco/7/GRCh38#149786972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435574-A-C

149786972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435574-A-G

http://identifiers.org/hco/7/GRCh38#149787056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435655-C-A

149787056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435655-C-T

149787061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435660-G-A

149787061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435660-G-C

149787061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435660-G-T

149787097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435684-T-A

149787097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435684-T-C

http://identifiers.org/hco/7/GRCh38#149787133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435721-A-C

149787133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435721-A-T

http://identifiers.org/hco/7/GRCh38#149787144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48435733-C-A

149787152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435741-G-T

149787167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435749-T-C

149787167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435749-T-G

149787216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435788-A-G

149787216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48435788-A-T

149787374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48435909-C-T

149787400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48435935-G-C

http://identifiers.org/hco/7/GRCh38#149787546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48436081-A-C

149787565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 48436100-G-A

149787565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 48436100-G-C

149787596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436155-G-A

149787596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436155-G-T

http://identifiers.org/hco/7/GRCh38#149787600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48436159-C-A

149787600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436159-C-T

149787708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48436278-G-A

149787708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48436278-G-T

149787725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48436295-T-C

http://identifiers.org/hco/7/GRCh38#149787789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48436359-C-A

http://identifiers.org/hco/7/GRCh38#149788108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48436678-C-A

149788108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436678-C-G

149788156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436725-C-T

http://identifiers.org/hco/7/GRCh38#149788225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48436796-C-A

149788225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436796-C-T

http://identifiers.org/hco/7/GRCh38#149788226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48436797-C-A

149788226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436797-C-T

149788231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436802-A-T

149788243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436814-T-A

http://identifiers.org/hco/7/GRCh38#149788302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48436872-C-A

149788302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48436872-C-T

149788323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 48436893-C-G

149788323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 48436893-C-T

149788427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48436997-C-G

http://identifiers.org/hco/7/GRCh38#149788506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48437063-C-A

149788507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437064-T-C

http://identifiers.org/hco/7/GRCh38#149788531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48437096-C-A

149788545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437112-G-A

149788545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437112-G-T

149788561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48437128-C-T

http://identifiers.org/hco/7/GRCh38#149788562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48437129-C-A

149788562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48437129-C-G

149788562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48437129-C-T

149788581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48437148-G-A

149788705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48437261-T-G

149788738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48437297-C-T

149788789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48437348-G-A

149788789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48437348-G-T

149788810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48437369-G-C

149788818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48437377-C-G

http://identifiers.org/hco/7/GRCh38#149788836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48437395-C-A

149788836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48437395-C-T

http://identifiers.org/hco/7/GRCh38#149789137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48437677-C-A

149789137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437677-C-T

149789153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437693-G-T

149789289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48437829-G-A

149789325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48437865-C-T

149789425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437964-G-A

149789425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437964-G-T

http://identifiers.org/hco/7/GRCh38#149789439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48437978-C-A

149789439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48437978-C-T

149789494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438029-G-A

149789494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438029-G-C

149789494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438029-G-T

149789498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438033-G-A

149789498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438033-G-C

149789498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438033-G-T

149789509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438045-T-C

149789528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438065-G-A

149789528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438065-G-T

http://identifiers.org/hco/7/GRCh38#149789588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48438392-C-A

149789588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438392-C-T

http://identifiers.org/hco/7/GRCh38#149789751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48438555-C-A

149789751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48438555-C-T

http://identifiers.org/hco/7/GRCh38#149789779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48438583-C-A

149789779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48438583-C-T

149789831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438635-C-T

149789853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438658-G-A

149789853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438658-G-T

http://identifiers.org/hco/7/GRCh38#149789862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48438667-C-A

149789878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438688-A-G

149789882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438692-G-A

149789882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438692-G-C

149789882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438692-G-T

149789905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438715-A-G

149790024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438808-G-A

http://identifiers.org/hco/7/GRCh38#149790037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48438824-C-A

149790043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48438830-G-T

149790061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48438848-T-C

149790072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438859-G-T

149790171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48438945-G-A

149790171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48438945-G-C

149790171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48438945-G-T

http://identifiers.org/hco/7/GRCh38#149790173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48438947-A-C

149790173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48438947-A-G

149790203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438977-G-A

149790203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48438977-G-T

149790255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48439019-G-T

149790258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48439022-G-C

149790258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48439022-G-T

http://identifiers.org/hco/7/GRCh38#149790277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439041-C-A

149790277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48439041-C-G

149790277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48439041-C-T

http://identifiers.org/hco/7/GRCh38#149790287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439051-A-C

149790287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439051-A-G

http://identifiers.org/hco/7/GRCh38#149790289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439053-C-A

149790289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439053-C-T

http://identifiers.org/hco/7/GRCh38#149790336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439100-C-A

149790336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439100-C-G

149790336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439100-C-T

http://identifiers.org/hco/7/GRCh38#149790424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439188-C-A

149790424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439188-C-T

149790485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439249-T-A

149790485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439249-T-C

149790533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439297-G-A

149790533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439297-G-T

149790550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439307-G-A

149790550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439307-G-C

149790550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439307-G-T

http://identifiers.org/hco/7/GRCh38#149790552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439309-C-A

149790552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439309-C-G

149790552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439309-C-T

149790558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439315-G-A

149790558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439315-G-C

149790558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48439315-G-T

149790624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48439388-G-A

149790624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48439388-G-T

149790667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48439425-T-A

http://identifiers.org/hco/7/GRCh38#149790739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439503-C-A

149790739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48439503-C-T

149790867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48439632-C-T

149790922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48439688-T-C

149790964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48439756-C-T

http://identifiers.org/hco/7/GRCh38#149790995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439822-A-C

149790995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48439822-A-G

149790995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48439822-A-T

149791026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48439857-G-A

149791026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48439857-G-T

149791035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48439869-G-A

149791035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48439869-G-T

http://identifiers.org/hco/7/GRCh38#149791043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48439877-C-A

149791043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48439877-C-T

149791093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440061-G-A

149791093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440061-G-C

149791093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440061-G-T

149791408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48440349-G-A

http://identifiers.org/hco/7/GRCh38#149791446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48440381-C-A

149791446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48440381-C-T

http://identifiers.org/hco/7/GRCh38#149791505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48440440-C-A

149791505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440440-C-T

149791510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440445-G-A

149791510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440445-G-T

http://identifiers.org/hco/7/GRCh38#149791525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48440460-C-A

149791525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440460-C-G

149791525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440460-C-T

149791573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440508-G-A

149791573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440508-G-C

149791573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440508-G-T

149791591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440526-T-C

http://identifiers.org/hco/7/GRCh38#149791604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48440539-C-A

149791604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440539-C-T

149791716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48440671-T-G

149791719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48440674-G-A

149791719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48440674-G-T

149791720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48440675-G-A

149791720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48440675-G-T

http://identifiers.org/hco/7/GRCh38#149791776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48440729-C-A

149791776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48440729-C-T

http://identifiers.org/hco/7/GRCh38#149791926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48440903-C-A

149791926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440903-C-T

http://identifiers.org/hco/7/GRCh38#149791948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48440925-C-A

149791948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440925-C-G

149791948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48440925-C-T

149791992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441069-C-T

http://identifiers.org/hco/7/GRCh38#149792059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441196-C-A

149792213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48441350-G-A

149792213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48441350-G-T

http://identifiers.org/hco/7/GRCh38#149792309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441423-C-A

149792309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441423-C-G

149792309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441423-C-T

http://identifiers.org/hco/7/GRCh38#149792470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441584-C-A

149792470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441584-C-T

149792512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441615-T-C

http://identifiers.org/hco/7/GRCh38#149792523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441658-C-A

149792523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441658-C-T

149792536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441685-A-G

http://identifiers.org/hco/7/GRCh38#149792555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441700-C-A

149792555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441700-C-T

149792593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441737-T-C

149792593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441737-T-G

http://identifiers.org/hco/7/GRCh38#149792604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441748-A-C

149792625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441769-C-G

149792625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441769-C-T

149792680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441824-C-T

149792718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48441862-C-T

http://identifiers.org/hco/7/GRCh38#149792783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441927-A-C

149792783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441927-A-G

149792783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441927-A-T

149792795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441939-G-A

http://identifiers.org/hco/7/GRCh38#149792829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441963-C-A

149792829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48441963-C-T

http://identifiers.org/hco/7/GRCh38#149792848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48441982-C-A

149792922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442025-C-G

149793023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442133-G-A

149793023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442133-G-C

149793162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442258-A-G

149793203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442293-A-G

http://identifiers.org/hco/7/GRCh38#149793247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48442324-C-A

149793247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442324-C-G

149793247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442324-C-T

http://identifiers.org/hco/7/GRCh38#149793282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48442359-C-A

149793282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442359-C-T

http://identifiers.org/hco/7/GRCh38#149793407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48442486-C-A

149793407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48442486-C-T

http://identifiers.org/hco/7/GRCh38#149793415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48442494-C-A

149793415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48442494-C-T

http://identifiers.org/hco/7/GRCh38#149793423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48442502-C-A

149793423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48442502-C-T

149793469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442548-G-A

149793606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48442706-A-G

149793676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48442774-T-C

http://identifiers.org/hco/7/GRCh38#149793692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48442790-A-C

149794645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443077-G-A

149794779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443210-A-G

149794891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443326-G-A

149794893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443328-C-G

149794893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443328-C-T

149794905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48443342-G-A

149794905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48443342-G-T

149794910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443347-G-A

http://identifiers.org/hco/7/GRCh38#149794997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48443425-C-A

149794997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443425-C-T

149795015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443444-G-A

149795015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443444-G-T

http://identifiers.org/hco/7/GRCh38#149795132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48443536-C-A

149795132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443536-C-G

149795134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443538-T-G

http://identifiers.org/hco/7/GRCh38#149795135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48443539-C-A

149795135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443539-C-T

149795184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443576-C-T

149795192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48443584-C-T

149795212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 48443610-C-G

149795267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443656-T-C

149795564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443916-C-T

http://identifiers.org/hco/7/GRCh38#149795569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48443921-A-C

149795569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443921-A-T

149795571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443923-G-A

149795571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443923-G-C

149795578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48443930-C-T

149795675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444027-C-T

149795690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444042-G-A

http://identifiers.org/hco/7/GRCh38#149795697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444049-C-A

149795697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444049-C-T

149795699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444051-G-T

http://identifiers.org/hco/7/GRCh38#149795725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444077-A-C

149795801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444152-G-T

149795806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444157-G-A

149795806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444157-G-T

http://identifiers.org/hco/7/GRCh38#149795818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444169-C-A

149795818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444169-C-T

http://identifiers.org/hco/7/GRCh38#149795828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444179-C-A

149795828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444179-C-T

149795888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444225-G-A

149795888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444225-G-T

149795897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444229-T-A

149795946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444286-G-A

149795961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444299-A-G

149795961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444299-A-T

http://identifiers.org/hco/7/GRCh38#149795970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444308-C-A

149795970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444308-C-T

149796020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444345-G-A

149796020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444345-G-T

149796052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444378-G-A

http://identifiers.org/hco/7/GRCh38#149796091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444397-C-A

149796091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444397-C-T

http://identifiers.org/hco/7/GRCh38#149796247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444436-C-A

149796247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444436-C-T

149796276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444459-G-A

149796346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48444507-A-T

http://identifiers.org/hco/7/GRCh38#149796418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444579-C-A

149796418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48444579-C-G

149796418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48444579-C-T

149796485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48444661-C-T

149796542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48444719-G-A

149796542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48444719-G-T

149796636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48444811-C-T

149796714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48444889-G-T

149796726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48444901-G-A

149796730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48444905-C-T

http://identifiers.org/hco/7/GRCh38#149796758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48444936-C-A

149796758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48444936-C-T

149796787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48444946-G-A

149796787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48444946-G-C

149796828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48444985-C-T

149796856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445000-A-G

149796888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445032-G-A

149796888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445032-G-T

149797048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445189-A-G

149797134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445271-A-G

149797159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445296-T-C

149797240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445359-C-T

http://identifiers.org/hco/7/GRCh38#149797249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445368-C-A

149797249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48445368-C-G

149797283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48445402-C-G

149797283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48445402-C-T

149797361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445469-G-T

http://identifiers.org/hco/7/GRCh38#149797400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445475-C-A

149797400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445475-C-T

149797418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445493-G-A

149797418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445493-G-T

http://identifiers.org/hco/7/GRCh38#149797425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445500-C-A

149797425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445500-C-T

149797447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445518-T-C

149797502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445613-G-A

149797502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445613-G-T

149797503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445614-G-A

149797503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445614-G-T

http://identifiers.org/hco/7/GRCh38#149797566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445670-C-A

149797566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445670-C-T

http://identifiers.org/hco/7/GRCh38#149797574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445688-C-A

149797574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445688-C-T

149797596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445710-C-T

149797637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445742-A-G

http://identifiers.org/hco/7/GRCh38#149797641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445746-C-A

149797641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445746-C-T

149797653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445759-C-G

http://identifiers.org/hco/7/GRCh38#149797656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445762-C-A

149797656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445762-C-T

149797702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445804-A-G

149797708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445810-G-T

149797715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445816-C-T

http://identifiers.org/hco/7/GRCh38#149797720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445821-A-C

149797750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445839-G-A

http://identifiers.org/hco/7/GRCh38#149797832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48445906-A-C

149797832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445906-A-G

149797865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445929-A-G

149797877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445941-G-A

149797877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48445941-G-T

http://identifiers.org/hco/7/GRCh38#149797953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446033-A-C

149797953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446033-A-G

149797977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446053-G-A

149797977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446053-G-T

149798087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48446110-A-G

http://identifiers.org/hco/7/GRCh38#149798158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446186-A-C

149798158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446186-A-G

http://identifiers.org/hco/7/GRCh38#149798170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446199-C-A

149798170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446199-C-G

149798170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446199-C-T

http://identifiers.org/hco/7/GRCh38#149798233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446235-C-A

149798233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446235-C-T

http://identifiers.org/hco/7/GRCh38#149798237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446239-A-C

http://identifiers.org/hco/7/GRCh38#149798241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446243-C-A

149798241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446243-C-G

149798241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446243-C-T

149798257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446259-G-T

149798289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446282-G-T

149798290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446283-A-G

149798409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446381-T-C

149798422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446394-G-T

149798450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446414-G-A

149798450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446414-G-T

149798468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446432-C-T

http://identifiers.org/hco/7/GRCh38#149798497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446460-C-A

http://identifiers.org/hco/7/GRCh38#149798511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446474-C-A

149798511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446474-C-T

149798556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446515-G-A

149798556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446515-G-C

149798574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446532-G-T

http://identifiers.org/hco/7/GRCh38#149798576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446534-C-A

149798576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446534-C-T

149798577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446535-A-G

149798613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446570-G-A

149798613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446570-G-C

149798651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446606-T-C

http://identifiers.org/hco/7/GRCh38#149798895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48446736-C-A

149798895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446736-C-T

149798909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446750-G-A

149798909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446750-G-T

149799031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446836-C-T

149799080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446885-G-A

149799080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48446885-G-T

149799083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48446888-A-T

149799100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48446898-G-T

149799358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447132-T-C

149799431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447198-G-T

149799714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447237-A-G

149799756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447273-C-T

http://identifiers.org/hco/7/GRCh38#149799772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48447292-C-A

149799772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447292-C-T

149799777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447296-T-C

149799819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447343-T-C

149799825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447349-C-T

149799871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447392-G-T

149799971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447492-C-G

149800025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447539-A-T

149800044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447554-G-A

149800044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447554-G-T

149800135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447646-C-T

149800147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447661-T-C

149800228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447744-A-G

149800228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447744-A-T

149800253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447769-G-A

149800253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447769-G-T

149800273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447793-G-A

149800273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48447793-G-T

149800293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447818-G-A

149800293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447818-G-T

http://identifiers.org/hco/7/GRCh38#149800312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48447837-C-A

149800312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447837-C-T

http://identifiers.org/hco/7/GRCh38#149800317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48447842-C-A

149800341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447866-C-T

149800375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447900-G-A

149800375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447900-G-T

149800387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447912-T-A

149800396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447921-G-A

149800396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48447921-G-T

149800511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448011-T-C

149800517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448017-T-A

149800517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448017-T-C

149800536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448035-G-T

149800542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448041-G-C

149800542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448041-G-T

http://identifiers.org/hco/7/GRCh38#149800549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48448048-C-A

http://identifiers.org/hco/7/GRCh38#149800772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48448243-A-C

149800772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448243-A-G

149801084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448617-A-T

149801105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448643-C-T

149801234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448777-T-A

149801236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48448779-T-A

149801532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449064-A-G

149801588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449154-G-T

149801723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449261-A-G

149801757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48449294-C-T

149801873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48449416-T-G

149801906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48449449-C-T

149801990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449530-G-A

149801990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449530-G-C

149801990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449530-G-T

http://identifiers.org/hco/7/GRCh38#149802086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48449629-C-A

149802086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48449629-C-T

149802122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48449665-G-T

149802267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449784-C-T

149802299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449794-T-C

149802299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48449794-T-G

149802836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450213-T-C

149802837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450214-G-A

149802837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450214-G-C

149802837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450214-G-T

149802854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450225-G-A

149802854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450225-G-T

149802855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450226-G-T

http://identifiers.org/hco/7/GRCh38#149802887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48450257-C-A

149802887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450257-C-T

149802980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450349-G-A

149802980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450349-G-T

http://identifiers.org/hco/7/GRCh38#149802982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48450351-C-A

149802982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450351-C-T

149803028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450397-G-A

149803028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450397-G-T

http://identifiers.org/hco/7/GRCh38#149803047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48450416-C-A

149803047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450416-C-G

149803047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450416-C-T

149803191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450552-A-T

149803246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450615-G-A

149803246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450615-G-T

149803433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450767-T-C

http://identifiers.org/hco/7/GRCh38#149803437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48450771-C-A

149803437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48450771-C-T

http://identifiers.org/hco/7/GRCh38#149803522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48450846-C-A

149803522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450846-C-T

149803576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48450900-T-C

http://identifiers.org/hco/7/GRCh38#149803612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48450989-C-A

149803612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48450989-C-T

http://identifiers.org/hco/7/GRCh38#149803670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48451066-C-A

149803709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48451105-G-A

149803709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48451105-G-T

149803797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48451193-G-C

149803835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451221-C-T

http://identifiers.org/hco/7/GRCh38#149803875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48451257-C-A

149803875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451257-C-T

149803911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451285-G-A

149803911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451285-G-T

149803918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451292-G-T

149803934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451305-G-A

149803934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451305-G-C

149803935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451306-A-G

149803947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451318-A-G

149804098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451472-G-A

149804127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451486-C-T

http://identifiers.org/hco/7/GRCh38#149804144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48451515-C-A

149804155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451526-T-C

149804155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451526-T-G

http://identifiers.org/hco/7/GRCh38#149804168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48451539-A-C

149804168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451539-A-G

http://identifiers.org/hco/7/GRCh38#149804217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48451666-C-A

149804217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451666-C-T

http://identifiers.org/hco/7/GRCh38#149804228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48451677-C-A

149804228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451677-C-G

149804228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451677-C-T

149804309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451757-G-A

149804435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48451870-C-T

149805300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452192-G-T

http://identifiers.org/hco/7/GRCh38#149805302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452194-C-A

149805302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452194-C-G

http://identifiers.org/hco/7/GRCh38#149805550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452431-C-A

149805550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48452431-C-T

http://identifiers.org/hco/7/GRCh38#149805725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452596-C-A

149805725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452596-C-T

http://identifiers.org/hco/7/GRCh38#149805734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452604-C-A

149805734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452604-C-T

149805747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452615-A-G

http://identifiers.org/hco/7/GRCh38#149805797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452650-C-A

149805797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452650-C-T

149805878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452706-G-T

http://identifiers.org/hco/7/GRCh38#149805901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452729-C-A

149805901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48452729-C-T

149805909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48452737-G-A

149805917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48452745-G-A

149806097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452921-G-A

149806097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452921-G-T

149806105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452927-T-A

http://identifiers.org/hco/7/GRCh38#149806133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452950-C-A

149806133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48452950-C-G

http://identifiers.org/hco/7/GRCh38#149806148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48452965-C-A

149806357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453116-A-G

149806375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453135-G-A

149806436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453188-C-T

http://identifiers.org/hco/7/GRCh38#149806479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48453230-C-A

149806601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453322-G-A

149806601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453322-G-T

http://identifiers.org/hco/7/GRCh38#149806625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48453338-C-A

149806625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453338-C-T

149806626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453339-G-A

149806626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453339-G-C

149806626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453339-G-T

149806640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453346-T-C

149806755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48453427-T-A

149806755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48453427-T-G

http://identifiers.org/hco/7/GRCh38#149806781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48453453-C-A

149807061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453751-T-C

149807061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48453751-T-G

149808391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48454621-C-T

http://identifiers.org/hco/7/GRCh38#149808574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48454795-C-A

149808574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48454795-C-T

http://identifiers.org/hco/7/GRCh38#149808578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48454799-C-A

149808700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48454938-G-T

http://identifiers.org/hco/7/GRCh38#149808727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48454956-C-A

149808727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48454956-C-G

http://identifiers.org/hco/7/GRCh38#149808728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48454957-C-A

149808728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48454957-C-T

http://identifiers.org/hco/7/GRCh38#149808739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48454964-C-A

149808739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48454964-C-G

http://identifiers.org/hco/7/GRCh38#149808774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48454982-C-A

149808774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48454982-C-T

149808912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455076-G-A

149808912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455076-G-T

http://identifiers.org/hco/7/GRCh38#149808959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48455136-C-A

149808959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455136-C-G

149808959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455136-C-T

149808997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455171-G-A

149808997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455171-G-T

149809346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455497-G-A

149809346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455497-G-T

http://identifiers.org/hco/7/GRCh38#149809422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48455578-A-C

149809422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48455578-A-G

149809453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48455609-T-C

http://identifiers.org/hco/7/GRCh38#149809526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48455682-C-A

149809526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48455682-C-G

149809526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48455682-C-T

149809560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455716-G-A

149809560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455716-G-C

149809560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455716-G-T

http://identifiers.org/hco/7/GRCh38#149809625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48455781-C-A

149809625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455781-C-G

149809625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48455781-C-T

149810651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456161-G-C

149810795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456294-G-A

149810795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456294-G-T

149810991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48456469-T-C

http://identifiers.org/hco/7/GRCh38#149811069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48456562-C-A

149811069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456562-C-T

http://identifiers.org/hco/7/GRCh38#149811181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48456675-C-A

149811190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456684-T-A

http://identifiers.org/hco/7/GRCh38#149811228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48456808-C-A

149811244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456879-C-T

149811249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456884-G-A

149811274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48456966-G-C

149811377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457054-T-C

149811506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457181-C-T

149811612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457283-G-A

149811612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457283-G-C

149811612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457283-G-T

149811636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457309-A-G

149811640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457313-A-G

149811652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457325-C-T

149811750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457421-T-G

149811776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457442-G-A

149811820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457482-G-A

http://identifiers.org/hco/7/GRCh38#149811875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48457523-C-A

149811875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457523-C-G

149811891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457534-G-A

149811993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48457636-C-G

149812095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48457738-A-G

149812132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457787-G-A

149812132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457787-G-C

149812132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457787-G-T

149812194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457823-T-C

http://identifiers.org/hco/7/GRCh38#149812240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48457867-C-A

149812240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48457867-C-T

http://identifiers.org/hco/7/GRCh38#149812341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48457968-C-A

149812341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48457968-C-T

149812354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48457981-C-T

http://identifiers.org/hco/7/GRCh38#149812360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48457987-C-A

149812360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48457987-C-T

149812453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458080-G-A

149812473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458098-A-G

149812503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458121-G-A

149812503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458121-G-T

149812575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48458185-G-A

149812726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458346-T-C

149812834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458440-A-G

149812894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458502-G-A

149812898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458506-T-C

149812990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458607-G-A

149812990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458607-G-C

http://identifiers.org/hco/7/GRCh38#149813042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48458703-C-A

149813112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458773-G-A

149813169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458845-A-T

149813196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458885-C-T

149813197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458886-G-A

149813298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48458982-A-G

149813351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459051-A-G

149813351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459051-A-T

149813420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48459121-C-T

149813464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459209-C-T

149813487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459309-T-C

http://identifiers.org/hco/7/GRCh38#149813502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48459327-C-A

149813502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459327-C-T

149813505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459330-T-C

149813505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459330-T-G

http://identifiers.org/hco/7/GRCh38#149813627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48459585-C-A

149813627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48459585-C-T

149813710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48459668-G-A

149813710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48459668-G-T

149813722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48459680-C-G

149813774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48459732-G-A

149813823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459790-G-A

149813823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459790-G-C

149813823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459790-G-T

149813828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459794-A-G

149813829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459795-G-A

149813829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459795-G-T

http://identifiers.org/hco/7/GRCh38#149813851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48459817-C-A

149813874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48459840-T-C

149814115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460032-A-G

149814218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460127-G-A

149814218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460127-G-T

149814221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460130-G-A

149814221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460130-G-T

149814234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460138-G-T

149814277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460178-G-A

149814277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460178-G-C

149814277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460178-G-T

149814300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460201-G-A

149814318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460218-T-C

http://identifiers.org/hco/7/GRCh38#149814331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48460226-C-A

149814331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48460226-C-T

149814397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460291-G-C

149814397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460291-G-T

149814405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460299-T-C

149814463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460367-T-A

149814463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460367-T-C

149814498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460402-G-A

149814498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460402-G-C

149814498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460402-G-T

149814593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460497-C-T

http://identifiers.org/hco/7/GRCh38#149814647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48460551-C-A

149814647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460551-C-T

149814648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460552-T-C

http://identifiers.org/hco/7/GRCh38#149814659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48460563-C-A

149814659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460563-C-T

http://identifiers.org/hco/7/GRCh38#149814682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48460585-C-A

149814682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460585-C-T

http://identifiers.org/hco/7/GRCh38#149814778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48460690-C-A

149814778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460690-C-G

149814778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48460690-C-T

http://identifiers.org/hco/7/GRCh38#149814972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48460894-C-A

149814972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460894-C-T

http://identifiers.org/hco/7/GRCh38#149814994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48460916-C-A

149814994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48460916-C-T

149815094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461012-G-T

149815115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461032-G-A

149815115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461032-G-T

149815463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461397-G-A

149815463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461397-G-T

149815623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461523-G-A

149815623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461523-G-T

http://identifiers.org/hco/7/GRCh38#149815708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48461587-C-A

149815708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48461587-C-G

149815708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48461587-C-T

http://identifiers.org/hco/7/GRCh38#149815711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48461590-C-A

149815711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48461590-C-T

149815819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461688-T-C

149815819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461688-T-G

149815826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461695-C-T

149815845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461714-G-T

149815861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461731-G-A

149815861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48461731-G-T

http://identifiers.org/hco/7/GRCh38#149815893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48461763-C-A

149815893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48461763-C-G

149815893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48461763-C-T

http://identifiers.org/hco/7/GRCh38#149815901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48461771-C-A

149815901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48461771-C-T

149815906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48461776-A-G

149816135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462007-A-G

http://identifiers.org/hco/7/GRCh38#149816214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48462077-A-C

149816214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462077-A-T

http://identifiers.org/hco/7/GRCh38#149816273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48462139-C-A

149816273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462139-C-T

149816288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462154-G-A

149816288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462154-G-T

149816338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462214-G-A

149816338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462214-G-C

149816338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462214-G-T

http://identifiers.org/hco/7/GRCh38#149816401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48462277-C-A

149816401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48462277-C-G

149816401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48462277-C-T

149816402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48462278-G-A

149816402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48462278-G-C

149816402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48462278-G-T

149816477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48462353-G-T

http://identifiers.org/hco/7/GRCh38#149816514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48462390-C-A

149816514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48462390-C-T

http://identifiers.org/hco/7/GRCh38#149816524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48462400-C-A

http://identifiers.org/hco/7/GRCh38#149816562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48462438-C-A

149816562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462438-C-T

149817011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462697-C-G

149817070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48462760-T-C

149817365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463007-C-T

149817440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463058-C-T

http://identifiers.org/hco/7/GRCh38#149817609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463225-C-A

149817609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463225-C-G

149817609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463225-C-T

http://identifiers.org/hco/7/GRCh38#149817615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463231-C-A

149817615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48463231-C-T

149817725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48463371-A-G

149817837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463467-G-A

http://identifiers.org/hco/7/GRCh38#149817864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463496-C-A

149817864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463496-C-T

149817884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463510-C-G

149817884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463510-C-T

149818010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48463644-C-T

http://identifiers.org/hco/7/GRCh38#149818016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463650-A-C

149818016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48463650-A-G

http://identifiers.org/hco/7/GRCh38#149818022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463656-A-C

http://identifiers.org/hco/7/GRCh38#149818113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463747-C-A

149818113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48463747-C-T

149818114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48463748-A-G

http://identifiers.org/hco/7/GRCh38#149818411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463933-C-A

149818411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48463933-C-T

http://identifiers.org/hco/7/GRCh38#149818445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48463967-C-A

http://identifiers.org/hco/7/GRCh38#149818599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48464098-C-A

149818599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464098-C-G

http://identifiers.org/hco/7/GRCh38#149818639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48464142-A-C

149818639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464142-A-G

149818639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464142-A-T

http://identifiers.org/hco/7/GRCh38#149818642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48464145-C-A

149818642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464145-C-T

149818683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48464190-C-G

149818683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48464190-C-T

149818744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48464251-C-T

149818924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464422-T-C

http://identifiers.org/hco/7/GRCh38#149818925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48464423-C-A

149818925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464423-C-T

http://identifiers.org/hco/7/GRCh38#149819044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48464545-A-C

149819104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464649-T-C

http://identifiers.org/hco/7/GRCh38#149819206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48464757-C-A

149819206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464757-C-T

149819242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464783-G-T

149819279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464816-T-G

149819280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48464817-G-T

149819400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48464930-G-A

149819400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48464930-G-T

149819471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48465001-C-G

149819471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48465001-C-T

149819530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465061-G-C

149819561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465105-T-C

149819572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465111-T-C

149819577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465127-T-C

149819588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465142-T-C

149819613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465168-G-A

149819613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465168-G-T

149819668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465215-G-A

149819668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465215-G-T

149819695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465242-G-A

149819695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48465242-G-T

149820548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48466163-G-A

149820548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48466163-G-T

149820570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48466185-A-G

149820570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48466185-A-T

http://identifiers.org/hco/7/GRCh38#149820639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48466623-C-A

149820639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48466623-C-T

http://identifiers.org/hco/7/GRCh38#149820717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48466699-C-A

149820826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48466808-G-A

149820913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48466896-G-A

149820913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48466896-G-T

149820937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48466920-G-A

149820937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48466920-G-T

http://identifiers.org/hco/7/GRCh38#149821026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467009-C-A

149821026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467009-C-T

http://identifiers.org/hco/7/GRCh38#149821041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467024-C-A

149821041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467024-C-T

http://identifiers.org/hco/7/GRCh38#149821106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467089-C-A

149821106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467089-C-T

149821180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467139-G-A

149821180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467139-G-T

149821209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467168-G-T

http://identifiers.org/hco/7/GRCh38#149821213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467172-C-A

149821213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467172-C-T

149821297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467255-G-A

149821297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467255-G-C

149821297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467255-G-T

149821350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467281-G-A

149821350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467281-G-T

149821355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467286-G-A

149821355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467286-G-T

http://identifiers.org/hco/7/GRCh38#149821400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467340-C-A

149821400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467340-C-T

149821406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467346-G-A

149821406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467346-G-C

149821406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467346-G-T

http://identifiers.org/hco/7/GRCh38#149821457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467397-C-A

149821457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467397-C-T

http://identifiers.org/hco/7/GRCh38#149821469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467409-C-A

http://identifiers.org/hco/7/GRCh38#149821511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467451-C-A

149821511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467451-C-T

http://identifiers.org/hco/7/GRCh38#149821562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467502-C-A

149821562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467502-C-G

149821562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467502-C-T

149821645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467584-T-C

149821743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48467653-G-A

http://identifiers.org/hco/7/GRCh38#149821773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467675-C-A

149821773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467675-C-T

http://identifiers.org/hco/7/GRCh38#149821799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467697-C-A

149821799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48467697-C-G

149821799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48467697-C-T

http://identifiers.org/hco/7/GRCh38#149821800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467698-C-A

149821800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48467698-C-T

149821867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48467757-G-A

149821867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48467757-G-C

149821867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 48467757-G-T

149822014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467913-C-T

http://identifiers.org/hco/7/GRCh38#149822026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48467925-C-A

149822026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467925-C-T

149822079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48467978-C-T

http://identifiers.org/hco/7/GRCh38#149822193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48468092-C-A

149822193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48468092-C-T

http://identifiers.org/hco/7/GRCh38#149822227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48468108-C-A

149822227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468108-C-T

149822387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468234-G-A

149822387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468234-G-T

149822528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48468359-C-T

149822548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48468379-G-A

149822548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48468379-G-C

149822548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48468379-G-T

149822564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48468395-G-A

149822790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468589-G-A

149822790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468589-G-T

149822817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48468608-G-A

149822817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48468608-G-T

149822820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468611-T-C

149823296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468979-G-A

149823296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48468979-G-T

149823365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469045-G-A

149823365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469045-G-T

149823384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469064-G-A

149823433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469113-A-G

149823592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469248-C-T

http://identifiers.org/hco/7/GRCh38#149823602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48469277-C-A

149823602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469277-C-G

149823602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469277-C-T

149823603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469278-G-A

149823609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469284-T-C

149823658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469335-G-A

149823664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469343-G-A

149823664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469343-G-T

http://identifiers.org/hco/7/GRCh38#149823782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48469475-C-A

149823782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469475-C-T

149823876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469572-G-A

149823876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469572-G-T

149823881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469577-G-A

149823881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469577-G-T

149823909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469625-G-A

149823909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469625-G-C

149823909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469625-G-T

149823935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469667-A-G

149823954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469684-G-A

149823954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469684-G-C

149823961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469691-G-A

149823961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469691-G-C

149823991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469720-G-T

149824069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48469780-A-G

149824087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48469798-G-A

149824087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48469798-G-T

149824097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469808-G-A

149824097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469808-G-T

http://identifiers.org/hco/7/GRCh38#149824305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48469990-C-A

149824305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48469990-C-T

http://identifiers.org/hco/7/GRCh38#149824376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48470058-C-A

149824376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470058-C-T

149824490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470172-A-T

149824588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470270-G-A

http://identifiers.org/hco/7/GRCh38#149824614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48470296-C-A

149824614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470296-C-T

149824678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470360-G-C

149824678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470360-G-T

149824686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470368-G-A

149824686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470368-G-T

149824714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470394-G-T

149824734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470410-T-A

149824734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470410-T-C

149824735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470411-G-A

149824735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470411-G-C

149824735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470411-G-T

http://identifiers.org/hco/7/GRCh38#149824738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48470414-C-A

149824738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470414-C-T

149824764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470443-T-A

149824764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470443-T-C

149824776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470469-C-T

149824803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470500-G-T

149824804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470501-G-T

149824808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470505-T-C

149824823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470518-G-T

http://identifiers.org/hco/7/GRCh38#149824850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48470545-C-A

149824850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470545-C-T

http://identifiers.org/hco/7/GRCh38#149824875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48470570-C-A

149824875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470570-C-T

149824877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470572-T-C

http://identifiers.org/hco/7/GRCh38#149824894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48470591-C-A

149824894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470591-C-T

149824910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470607-T-C

149824913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470610-A-G

149824913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470610-A-T

149824935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470642-T-C

149824949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470658-A-G

http://identifiers.org/hco/7/GRCh38#149825017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48470731-C-A

149825074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470788-C-G

149825074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48470788-C-T

149825204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48470921-C-T

http://identifiers.org/hco/7/GRCh38#149825435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471144-C-A

149825435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48471144-C-T

http://identifiers.org/hco/7/GRCh38#149825447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471156-C-A

149825447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471156-C-G

149825447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471156-C-T

149825528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48471222-G-T

149825558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471251-C-G

149825671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471462-T-G

149825674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471465-G-T

149825678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471469-G-A

149825678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471469-G-T

http://identifiers.org/hco/7/GRCh38#149825693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471484-C-A

149825693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471484-C-T

149825735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471514-G-T

http://identifiers.org/hco/7/GRCh38#149825751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471530-C-A

149825751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471530-C-T

http://identifiers.org/hco/7/GRCh38#149825757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471536-C-A

149825757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471536-C-T

http://identifiers.org/hco/7/GRCh38#149825790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471639-A-C

149825791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471675-C-T

http://identifiers.org/hco/7/GRCh38#149825795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471679-C-A

149825795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48471679-C-T

149825832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48471790-G-A

149825832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48471790-G-T

149825846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48471804-G-A

149825885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48471843-T-A

149825945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48471907-C-T

149825961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471922-G-T

http://identifiers.org/hco/7/GRCh38#149825984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48471946-C-A

149825984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48471946-C-T

149826072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48472039-C-G

149826072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48472039-C-T

149826170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48472137-G-A

http://identifiers.org/hco/7/GRCh38#149826432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48473052-C-A

149826432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48473052-C-T

149826470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473090-C-T

149826496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473116-G-A

149826496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473116-G-T

http://identifiers.org/hco/7/GRCh38#149826500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48473120-C-A

149826500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473120-C-T

149826537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473157-A-G

149826537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473157-A-T

149826539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473159-G-A

149826539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473159-G-T

149826641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473278-G-T

149826691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473326-G-A

149826691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473326-G-T

149826696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473331-G-A

149826696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473331-G-T

http://identifiers.org/hco/7/GRCh38#149826726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48473361-C-A

149826726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473361-C-G

149826726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473361-C-T

149826753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473388-C-G

149826753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473388-C-T

149826775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473410-C-G

149826828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48473463-G-A

149826828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48473463-G-T

149826948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473588-T-C

149827095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473701-T-C

http://identifiers.org/hco/7/GRCh38#149827119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48473725-C-A

149827119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473725-C-G

149827123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473729-T-A

149827123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473729-T-C

149827140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473746-G-A

http://identifiers.org/hco/7/GRCh38#149827143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48473749-C-A

149827143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473749-C-T

149827146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473752-A-G

149827181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473773-G-T

149827300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473882-C-T

149827378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473914-C-T

http://identifiers.org/hco/7/GRCh38#149827383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48473919-C-A

149827383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473919-C-G

149827383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48473919-C-T

149827439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474000-G-A

149827439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474000-G-C

http://identifiers.org/hco/7/GRCh38#149827442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48474003-C-A

149827442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474003-C-G

149827442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474003-C-T

http://identifiers.org/hco/7/GRCh38#149827446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48474007-C-A

http://identifiers.org/hco/7/GRCh38#149827461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48474019-C-A

149827461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474019-C-G

149827461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474019-C-T

149827512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474069-G-A

149827512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474069-G-T

149827513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474070-G-T

http://identifiers.org/hco/7/GRCh38#149827524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48474080-A-C

149827524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474080-A-G

149827539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474097-G-T

149827585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474128-A-G

149827629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474165-A-G

149827635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474171-A-G

149827648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474184-G-A

149827648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474184-G-T

149827650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474186-A-G

149827650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474186-A-T

149827665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474201-A-G

149827691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474230-G-A

149827691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474230-G-T

149827706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474252-G-A

149827706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48474252-G-T

http://identifiers.org/hco/7/GRCh38#149828080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48474591-A-C

149828080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48474591-A-G

http://identifiers.org/hco/7/GRCh38#149828112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48474619-C-A

149828112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48474619-C-T

149828605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475016-G-A

149828605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475016-G-T

http://identifiers.org/hco/7/GRCh38#149828618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475029-C-A

149828619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475030-T-A

149828619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475030-T-C

http://identifiers.org/hco/7/GRCh38#149828625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475036-C-A

http://identifiers.org/hco/7/GRCh38#149828628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475039-C-A

149828628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475039-C-T

http://identifiers.org/hco/7/GRCh38#149828634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475041-C-A

149828634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48475041-C-T

149828664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475071-T-C

149828664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475071-T-G

http://identifiers.org/hco/7/GRCh38#149828674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475081-C-A

149828674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475081-C-T

149828688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475095-G-T

149828691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475098-G-A

149828691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475098-G-T

149828695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475102-G-A

149828695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475102-G-C

149828695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48475102-G-T

http://identifiers.org/hco/7/GRCh38#149828850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475189-C-A

149828850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475189-C-T

http://identifiers.org/hco/7/GRCh38#149828904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475235-C-A

149828904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475235-C-G

149828904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475235-C-T

149828916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475247-G-A

149828916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475247-G-C

149828916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475247-G-T

149829001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475332-G-A

149829001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475332-G-T

149829028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475356-G-A

149829028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475356-G-T

http://identifiers.org/hco/7/GRCh38#149829055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475383-C-A

149829055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475383-C-G

149831032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475504-T-C

149831032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475504-T-G

http://identifiers.org/hco/7/GRCh38#149831034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475506-A-C

149831034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475506-A-G

149831034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475506-A-T

149831040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475512-T-A

149831040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475512-T-C

149831040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475512-T-G

http://identifiers.org/hco/7/GRCh38#149831055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475520-C-A

149831055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475520-C-T

http://identifiers.org/hco/7/GRCh38#149831056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475521-C-A

149831056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475521-C-T

http://identifiers.org/hco/7/GRCh38#149831100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475566-C-A

149831100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475566-C-T

149831294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475737-G-A

http://identifiers.org/hco/7/GRCh38#149831326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475765-C-A

149831326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475765-C-T

http://identifiers.org/hco/7/GRCh38#149831329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475766-C-A

149831329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475766-C-T

http://identifiers.org/hco/7/GRCh38#149831330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475767-C-A

149831330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475767-C-T

http://identifiers.org/hco/7/GRCh38#149831336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475773-C-A

149831336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475773-C-T

http://identifiers.org/hco/7/GRCh38#149831337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475774-C-A

http://identifiers.org/hco/7/GRCh38#149831381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475825-C-A

149831381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475825-C-G

http://identifiers.org/hco/7/GRCh38#149831394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48475838-C-A

149831394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475838-C-T

149831408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475849-A-G

149831446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48475888-C-T

149832031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48476293-G-C

149832034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48476296-G-A

149832034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48476296-G-T

149832057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48476317-C-T

149832622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477168-G-T

149832644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477189-A-G

149832755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477292-C-G

149832755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477292-C-T

149832756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477293-C-T

149832854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48477391-G-A

149832854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48477391-G-T

149832879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48477416-C-T

http://identifiers.org/hco/7/GRCh38#149832946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48477481-C-A

149832946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477481-C-T

http://identifiers.org/hco/7/GRCh38#149833002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48477566-C-A

149833002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477566-C-T

149833006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477570-T-C

http://identifiers.org/hco/7/GRCh38#149833039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48477600-C-A

149833039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477600-C-T

149833051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477616-T-C

http://identifiers.org/hco/7/GRCh38#149833053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48477618-C-A

149833053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477618-C-T

http://identifiers.org/hco/7/GRCh38#149833058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48477623-C-A

149833058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477623-C-T

http://identifiers.org/hco/7/GRCh38#149833204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48477716-A-C

149833204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477716-A-G

149833204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477716-A-T

149833752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48477961-A-G

149833838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478042-G-A

149833838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478042-G-T

149833850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478054-C-T

http://identifiers.org/hco/7/GRCh38#149833880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48478084-C-A

149833880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478084-C-T

http://identifiers.org/hco/7/GRCh38#149833893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48478097-C-A

149833893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478097-C-T

149833918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478122-G-T

149833925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478129-A-G

149833925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21998
most severe consequence: non coding transcript exon variant
orthologous variants: 48478129-A-T