http://identifiers.org/hco/1/GRCh38#16124579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141056449-C-A

16124580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141056448-C-T

http://identifiers.org/hco/1/GRCh38#16124621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141056410-C-A

16124856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141056180-T-A

16124856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141056180-T-C

16124871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141056165-G-T

http://identifiers.org/hco/1/GRCh38#16124876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141056158-C-A

16124876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141056158-C-T

16124994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141056037-A-T

16125065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141055971-G-A

16125065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141055971-G-T

16125188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3 prime UTR variant
orthologous variants: 141055843-C-T

16125297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141055745-C-G

16125297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141055745-C-T

16125325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 141055717-G-A

http://identifiers.org/hco/1/GRCh38#16125379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141055661-C-A

16125379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141055661-C-G

16125379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141055661-C-T

16125409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141055631-G-A

16125409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141055631-G-T

http://identifiers.org/hco/1/GRCh38#16125672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141054078-A-C

16126490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141054703-A-G

16126537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141054743-G-T

16127227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141053648-T-C

http://identifiers.org/hco/1/GRCh38#16127279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141053612-C-A

16127396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141053501-T-C

16127770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141053195-A-G

16128213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141052739-G-A

16128542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141052423-C-T

16128696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141052271-T-C

http://identifiers.org/hco/1/GRCh38#16128824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141052186-A-C

16129160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141052041-C-T

16129237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051965-G-A

16129400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051725-G-T

16129421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051708-G-C

16129464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141051666-G-A

16129554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141051576-T-C

16129559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: synonymous variant
orthologous variants: 141051571-G-A

16129559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: synonymous variant
orthologous variants: 141051571-G-C

16129559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: synonymous variant
orthologous variants: 141051571-G-T

16129668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051472-G-T

http://identifiers.org/hco/1/GRCh38#16129689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141051452-C-A

16129689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051452-C-G

16129689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051452-C-T

http://identifiers.org/hco/1/GRCh38#16129743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141051397-A-C

16129743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051397-A-G

16129839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051328-A-G

16129880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051286-A-G

16130094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051101-A-G

16130094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051101-A-T

http://identifiers.org/hco/1/GRCh38#16130124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141051014-C-A

16130124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051014-C-G

16130124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051014-C-T

http://identifiers.org/hco/1/GRCh38#16130129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141051009-C-A

16130129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051009-C-G

16130129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051009-C-T

http://identifiers.org/hco/1/GRCh38#16130130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141051008-C-A

16130130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051008-C-T

http://identifiers.org/hco/1/GRCh38#16130133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141051005-C-A

16130136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051002-G-A

16130136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051002-G-C

16130136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141051002-G-T

16130268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141050873-C-T

16130298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141050843-T-A

16130298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141050843-T-C

16130310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141050831-G-A

16130379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141050762-G-A

16130382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141050759-G-A

16130425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 141050716-G-A

16130429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050712-C-T

16130483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050657-A-T

16130484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050656-G-A

16130484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050656-G-T

16130489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050652-T-A

16130489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050652-T-C

16130493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050648-G-C

16130493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050648-G-T

16130609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050540-G-C

16131710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141050064-A-G

16131789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141049976-A-G

16131806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141049959-G-A

16131873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 141049892-G-A

16131907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141049860-C-T

16131957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141049810-C-T

http://identifiers.org/hco/1/GRCh38#16132032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141049760-C-A

16132049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141049738-C-T

16132092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141049693-T-A

http://identifiers.org/hco/1/GRCh38#16132104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141049681-C-A

16132104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141049681-C-T

16132182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141049603-A-G

16132215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141049570-G-C

http://identifiers.org/hco/1/GRCh38#16132314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141049479-C-A

16132314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141049479-C-G

16132314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141049479-C-T

http://identifiers.org/hco/1/GRCh38#16132358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141049453-C-A

16132358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141049453-C-G

16133079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141049324-G-A

16133079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141049324-G-T

16133080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141049322-G-T

16133101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141049313-G-A

16133101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141049313-G-T

16133106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141049308-G-A

16133106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141049308-G-T

16133202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 141049177-G-A

16133221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141049158-C-G

16133221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141049158-C-T

16133424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048952-C-G

16133424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048952-C-T

16133432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048950-G-C

16133619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048761-G-A

16133621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048759-G-C

16133621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048759-G-T

http://identifiers.org/hco/1/GRCh38#16133652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141048728-C-A

16133652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048728-C-T

16133678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048702-A-G

16133703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048669-T-G

http://identifiers.org/hco/1/GRCh38#16133810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141048617-C-A

16133810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048617-C-T

16133839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048599-G-A

16133840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048598-G-A

16133840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141048598-G-T

16133943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 141048498-G-A

http://identifiers.org/hco/1/GRCh38#16133949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141048493-A-C

16133975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 141048467-G-A

http://identifiers.org/hco/1/GRCh38#16134042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141048412-C-A

16134042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 141048412-C-T

16134162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, stop_retained_variant
orthologous variants: 141048361-T-C

http://identifiers.org/hco/1/GRCh38#16134163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, stop_lost
orthologous variants: http://identifiers.org/mco/4/GRCm39#141048360-A-C

16134510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141047860-A-G

16134510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense variant
orthologous variants: 141047860-A-T

http://identifiers.org/hco/1/GRCh38#16134605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141047771-C-A

http://identifiers.org/hco/1/GRCh38#16134853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141046517-C-A

16134869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141046504-C-T

16134895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141046498-G-A

16134895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141046498-G-T

http://identifiers.org/hco/1/GRCh38#16134899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141046494-C-A

http://identifiers.org/hco/1/GRCh38#16134900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141046493-C-A

16134900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141046493-C-T

16134974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141046419-G-C

16134974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141046419-G-T

16135083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141046338-T-C

16135113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141046308-G-T

16135155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141046266-T-C

http://identifiers.org/hco/1/GRCh38#16135513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141046011-C-A

16135532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045992-A-G

16135532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045992-A-T

16135555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045969-G-A

16135555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045969-G-T

16135558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045966-T-A

16135580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045949-G-T

16135638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045918-G-A

16135638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045918-G-C

16135638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045918-G-T

http://identifiers.org/hco/1/GRCh38#16135785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141045776-C-A

16135785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045776-C-T

16135792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045770-G-A

16135792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141045770-G-T

16137788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141044573-G-T

16137832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141044531-G-T

http://identifiers.org/hco/1/GRCh38#16138020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141044345-C-A

16138021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141044344-T-C

16138167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141044198-T-C

16138470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141043863-T-C

http://identifiers.org/hco/1/GRCh38#16138595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141043815-C-A

http://identifiers.org/hco/1/GRCh38#16138655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141043762-C-A

16138831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141043631-C-G

16138831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141043631-C-T

16138926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141043562-T-G

16139153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141043344-G-A

16139278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141043229-G-A

http://identifiers.org/hco/1/GRCh38#16139300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141043207-C-A

16139511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141043054-T-C

http://identifiers.org/hco/1/GRCh38#16139512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141043053-C-A

16139749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141042861-T-G

16139842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141042769-G-C

16139965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141042648-C-G

16139965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141042648-C-T

16140108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141042522-G-A

16140578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141042098-C-T

16141138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041992-A-G

16141165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041965-G-A

16141233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041933-G-C

16141279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041921-G-A

16141320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041882-G-A

16141374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041842-T-A

16141388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041829-C-T

16141417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041799-C-T

16142054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041216-C-T

16142172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141041150-C-G

16142391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040895-A-G

16142528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040745-T-C

16142558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040715-G-A

16142582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040690-G-T

16142594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040678-A-G

16143282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040639-G-C

16143438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040510-G-A

16143520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040432-T-G

16143599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040353-G-C

16143820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040141-G-A

16143904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141040086-G-A

16144294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039768-T-G

16144329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039744-G-A

16144375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039697-A-G

16144455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039664-G-A

16144706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039473-G-C

16144775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039419-G-A

16144986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039246-G-A

16144987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141039245-T-C

16145335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141038964-G-C

16145505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141038786-C-T

16146289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141037986-G-A

16146488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037789-G-A

16146488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037789-G-T

http://identifiers.org/hco/1/GRCh38#16146519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141037765-C-A

16146519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037765-C-T

http://identifiers.org/hco/1/GRCh38#16146531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141037753-C-A

16146531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037753-C-T

16146538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037746-A-T

16146912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037405-G-C

16146980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037322-G-A

16147258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141037055-C-T

16148363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141036404-A-T

16148364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron variant
orthologous variants: 141036403-G-C

16148435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141036332-G-A

16148435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141036332-G-C

16148435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141036332-G-T

16148473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141036294-G-A

16148746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141036015-A-G

16148857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141035904-C-T

16148871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 141035890-A-T

16149072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035685-T-C

16149077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035680-G-A

16149077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035680-G-T

16149080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035677-G-A

16149080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035677-G-T

16149173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035438-T-A

16149173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035438-T-C

16149500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035170-C-T

16149519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035152-G-A

16149519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141035152-G-T

http://identifiers.org/hco/1/GRCh38#16149546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141035135-A-C

16149823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034780-A-G

16149866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034721-C-T

16149898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034678-T-G

16149943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034648-G-A

16150039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034548-C-T

16150183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034422-C-T

16150756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034012-G-A

16150756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141034012-G-T

16151117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141033693-C-T

16151438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141033431-C-T

http://identifiers.org/hco/1/GRCh38#16151454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141033415-C-A

16151454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141033415-C-G

16151814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141032871-A-T

16151929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141032736-T-C

16151929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141032736-T-G

http://identifiers.org/hco/1/GRCh38#16152056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141032633-A-C

16152216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141032450-G-A

16152671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141031551-C-G

16152770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141031463-G-A

16152860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141031406-C-G

16152880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141031389-C-T

http://identifiers.org/hco/1/GRCh38#16153004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141031289-C-A

16153004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141031289-C-G

16153004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141031289-C-T

16153049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141031241-C-T

16153290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141031087-C-G

16153297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141031080-G-A

16153297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141031080-G-T

16153351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141031026-G-A

16153351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141031026-G-T

16153442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141030942-G-A

16153442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141030942-G-T

16153843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141030417-C-T

16154147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141030107-C-G

16154556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141029883-T-C

16154783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141029838-A-G

16154805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141029817-G-C

16155099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141029498-C-T

16155252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029345-G-A

16155252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029345-G-T

16155256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029341-G-T

16155303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029296-C-G

16155341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029252-G-A

16155341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029252-G-T

16155378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029212-C-T

16155415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029194-T-A

16155492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029112-G-A

16155492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029112-G-T

http://identifiers.org/hco/1/GRCh38#16155494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141029109-C-A

16155494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029109-C-G

16155494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029109-C-T

http://identifiers.org/hco/1/GRCh38#16155517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141029086-C-A

16155517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029086-C-T

16155531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029072-A-G

16155531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029072-A-T

http://identifiers.org/hco/1/GRCh38#16155537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141029066-C-A

16155537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029066-C-T

16155576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029029-G-T

16155595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029010-T-A

16155595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141029010-T-C

16155652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028953-T-C

16155652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028953-T-G

16155669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028937-T-C

http://identifiers.org/hco/1/GRCh38#16155670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141028936-A-C

16155670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028936-A-G

16155757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 141028844-T-C

16155777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028824-G-A

16155777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028824-G-T

16155790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028811-G-A

16155790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028811-G-C

16155790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028811-G-T

http://identifiers.org/hco/1/GRCh38#16155812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141028789-C-A

16155812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028789-C-T

http://identifiers.org/hco/1/GRCh38#16155820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141028781-C-A

16155820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028781-C-T

16155833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028764-G-A

16155833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028764-G-C

16155833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141028764-G-T

16155903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 141028691-G-A

16155903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028691-G-C

16155903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028691-G-T

http://identifiers.org/hco/1/GRCh38#16155913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141028681-C-A

16155913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028681-C-T

http://identifiers.org/hco/1/GRCh38#16155946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141028648-C-A

16155946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028648-C-T

http://identifiers.org/hco/1/GRCh38#16155992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141028628-C-A

16155992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028628-C-G

16155998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028622-G-A

16155998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028622-G-C

16155998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028622-G-T

16156031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028588-T-C

16156032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028587-G-A

16156032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141028587-G-T