http://identifiers.org/hco/1/GRCh38#156525935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88028057-C-A

156525935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88028057-C-T

http://identifiers.org/hco/1/GRCh38#156525975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88028017-C-A

156526013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88027976-C-T

156526034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88027956-A-G

http://identifiers.org/hco/1/GRCh38#156526051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027939-A-C

156526051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88027939-A-G

156526051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88027939-A-T

156526146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88027858-T-C

156526166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88027828-G-A

http://identifiers.org/hco/1/GRCh38#156526201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027794-C-A

http://identifiers.org/hco/1/GRCh38#156526239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027768-C-A

156526269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027746-A-G

http://identifiers.org/hco/1/GRCh38#156526273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027742-C-A

http://identifiers.org/hco/1/GRCh38#156526402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027657-C-A

156526402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027657-C-T

156526403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027656-T-C

156526406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027653-A-G

156526406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027653-A-T

http://identifiers.org/hco/1/GRCh38#156526433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027629-A-C

156526433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027629-A-G

156526433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027629-A-T

156526465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027599-G-A

156526465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027599-G-T

156526467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027597-G-A

156526468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027596-T-C

156526468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027596-T-G

156526479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027588-G-A

156526479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88027588-G-T

http://identifiers.org/hco/1/GRCh38#156526496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027571-A-C

156526647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88027420-G-T

156526648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88027419-T-A

http://identifiers.org/hco/1/GRCh38#156526693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88027380-C-A

156526693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88027380-C-T

http://identifiers.org/hco/1/GRCh38#156528004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88025037-A-C

156528084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024957-A-T

156528150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024908-A-G

156528362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024727-G-A

156528362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024727-G-T

156528363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024726-G-T

156528367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024722-G-A

156528367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024722-G-C

156528367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024722-G-T

156528581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88024533-G-C

http://identifiers.org/hco/1/GRCh38#156528641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88024477-C-A

156528643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024475-A-G

http://identifiers.org/hco/1/GRCh38#156528682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88024446-C-A

156528682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024446-C-T

156528722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024409-T-C

156528759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024384-A-G

156528819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024344-T-C

156528970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88024197-T-C

156529027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88024140-A-G

156529167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024031-A-G

http://identifiers.org/hco/1/GRCh38#156529181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88024017-C-A

156529181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024017-C-G

156529181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88024017-C-T

156530017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88023488-G-A

156530017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88023488-G-T

http://identifiers.org/hco/1/GRCh38#156530051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88023474-C-A

156530051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88023474-C-T

156530312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88023214-T-G

156530343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88023180-G-A

156530343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88023180-G-T

156530752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022662-G-A

156530891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022536-G-A

156530918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022518-C-T

156531283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022186-G-C

156531283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022186-G-T

156531333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022140-T-A

156531333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022140-T-C

http://identifiers.org/hco/1/GRCh38#156531355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88022118-C-A

156531355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022118-C-T

156531369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022094-G-A

156531369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022094-G-C

156531374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022089-G-A

156531374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022089-G-C

http://identifiers.org/hco/1/GRCh38#156531375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88022088-A-C

156531375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022088-A-T

156531376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022087-G-A

156531376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022087-G-C

156531376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022087-G-T

156531448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88022016-G-A

156532710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88021605-G-A

156532755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88021560-C-T

156532869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88021454-G-T

156533288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88021093-G-A

156533359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88021049-C-G

156533475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020977-T-C

http://identifiers.org/hco/1/GRCh38#156533624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88020842-C-A

156533624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020842-C-G

156533652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020812-A-G

156533737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020777-C-T

156533899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020629-A-G

156534018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88020528-G-A

156534169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020354-G-A

156534169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020354-G-T

156534355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020239-C-T

http://identifiers.org/hco/1/GRCh38#156534375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88020224-A-C

156534375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020224-A-G

156534459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020172-G-T

156534472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020156-A-G

http://identifiers.org/hco/1/GRCh38#156534478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88020150-C-A

156534478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020150-C-G

156534478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88020150-C-T

156534633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88020003-G-A

156534633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88020003-G-C

156534652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88019984-C-G

156534652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88019984-C-T

156534729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88019907-A-T

http://identifiers.org/hco/1/GRCh38#156535030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88019810-A-C

156535030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019810-A-G

156535030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019810-A-T

http://identifiers.org/hco/1/GRCh38#156535051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88019789-C-A

156535051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019789-C-T

http://identifiers.org/hco/1/GRCh38#156535120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88019734-C-A

156535120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019734-C-T

http://identifiers.org/hco/1/GRCh38#156535314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88019552-C-A

156535314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019552-C-T

156535344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019523-G-A

156535344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019523-G-C

156535344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019523-G-T

http://identifiers.org/hco/1/GRCh38#156535356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88019511-C-A

156535356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019511-C-T

156535657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88019112-A-G

156536045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88018657-C-T

http://identifiers.org/hco/1/GRCh38#156536994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88017591-C-A

156536994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88017591-C-T

156537033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88017553-A-G

http://identifiers.org/hco/1/GRCh38#156537103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88017499-C-A

http://identifiers.org/hco/1/GRCh38#156537377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88017247-C-A

156537429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88017204-G-A

156537429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88017204-G-T

http://identifiers.org/hco/1/GRCh38#156537439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88017194-C-A

156537547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88017063-T-C

156538719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88016857-T-C

156539039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88016571-G-T

156539079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88016537-G-C

156539079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88016537-G-T

156539177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88016438-G-T

156539198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88016417-T-C

http://identifiers.org/hco/1/GRCh38#156539202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88016414-C-A

156539210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88016406-G-A

156539210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88016406-G-T

http://identifiers.org/hco/1/GRCh38#156539428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88016221-C-A

156539428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88016221-C-G

156539428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88016221-C-T

156539437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88016212-G-T

156539548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88016101-G-C

156539551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88016098-G-A

http://identifiers.org/hco/1/GRCh38#156539851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88015805-A-C

156539996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 88015662-G-A

http://identifiers.org/hco/1/GRCh38#156540041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88015617-C-A

156540041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88015617-C-T

156540155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88015548-A-T

156540507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88015203-G-T

156540901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88014832-G-C

156540904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88014829-T-A

http://identifiers.org/hco/1/GRCh38#156540998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88014747-C-A

156540998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88014747-C-T

156541258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88014562-C-T

156541309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88014510-C-T

156543271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88012471-A-G

156543275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88012467-C-T

156543557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88012171-G-A

http://identifiers.org/hco/1/GRCh38#156543899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88011895-C-A

156543899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88011895-C-T

156543915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88011878-G-T

156544040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88011781-A-G

http://identifiers.org/hco/1/GRCh38#156544056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88011765-A-C

156544094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88011722-C-T

156544168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88011661-T-C

156544216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88011613-G-A

156544216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88011613-G-T

http://identifiers.org/hco/1/GRCh38#156544236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88011593-A-C

156544236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88011593-A-G

http://identifiers.org/hco/1/GRCh38#156544550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88011306-C-A

156544550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88011306-C-G

156544550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88011306-C-T

156547686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88009658-T-C

156547922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88009500-T-C

156547926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88009496-T-A

156547982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88009440-A-G

156548058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88009386-G-A

156548085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88009360-G-T

http://identifiers.org/hco/1/GRCh38#156548202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88009243-C-A

156548202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88009243-C-T

156548221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88009224-G-A

156548336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88009134-G-T

156548406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 88009064-C-T

156548500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008969-C-G

156548562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008920-G-A

156548616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88008865-G-A

156548634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88008847-G-A

156548634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88008847-G-C

156548818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008667-A-G

156548843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008646-G-A

156548843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008646-G-T

156548907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008606-T-G

156548971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008556-G-A

156550230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008046-C-T

156550239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008037-G-T

http://identifiers.org/hco/1/GRCh38#156550241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88008035-C-A

156550241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88008035-C-T

156550269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88008013-G-T

http://identifiers.org/hco/1/GRCh38#156550302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88007980-C-A

156550302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88007980-C-G

156550401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007873-T-A

156550401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007873-T-C

http://identifiers.org/hco/1/GRCh38#156550432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88007845-C-A

156550441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007836-G-A

156550446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007831-G-A

156550446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007831-G-T

http://identifiers.org/hco/1/GRCh38#156550457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88007821-C-A

156550460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007818-A-G

156550577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007716-C-T

156550710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007615-G-T

156550771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007560-G-A

156550959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88007418-C-G

156551229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88006747-G-A

156551288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88006707-C-T

http://identifiers.org/hco/1/GRCh38#156551593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88006447-C-A

http://identifiers.org/hco/1/GRCh38#156551602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88006436-C-A

156551602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88006436-C-T

156551655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88006379-G-A

156551655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88006379-G-T

156551879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88006153-G-C

http://identifiers.org/hco/1/GRCh38#156552101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88005617-A-C

156552101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 88005617-A-G

http://identifiers.org/hco/1/GRCh38#156552130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88005595-C-A

http://identifiers.org/hco/1/GRCh38#156552192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88005553-A-C

http://identifiers.org/hco/1/GRCh38#156552195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88005550-A-C

http://identifiers.org/hco/1/GRCh38#156552196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88005549-C-A

156552196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88005549-C-T

http://identifiers.org/hco/1/GRCh38#156552205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88005540-C-A

156552324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88005447-T-G

156552409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88005369-C-G

http://identifiers.org/hco/1/GRCh38#156552415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88005364-C-A

156552728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88005090-C-T

http://identifiers.org/hco/1/GRCh38#156554090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88004462-C-A

156554219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88004384-G-A

156554339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 88004260-G-C

156554360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 88004239-C-T

http://identifiers.org/hco/1/GRCh38#156554458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88004154-C-A

156554458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88004154-C-T

156554469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88004143-G-A

156554469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88004143-G-T

156555785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88002621-C-T

156555825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88002600-A-G

156556056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88002391-C-T

156556636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88001946-G-A

156556656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88001926-C-T

156556733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001849-T-G

156556749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001834-C-G

156556749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001834-C-T

156556752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001831-T-C

156556752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001831-T-G

http://identifiers.org/hco/1/GRCh38#156556761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88001822-A-C

156556761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001822-A-G

156556861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001721-G-C

http://identifiers.org/hco/1/GRCh38#156559483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88001329-A-C

156559483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001329-A-G

156559555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001289-G-A

156559665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001189-G-A

156559804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88001005-G-A

156559866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88000915-T-C

156560802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999925-G-A

156560802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999925-G-T

http://identifiers.org/hco/1/GRCh38#156560815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87999912-C-A

156560815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999912-C-T

http://identifiers.org/hco/1/GRCh38#156560847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87999875-C-A

156560868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999854-G-A

156560868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999854-G-C

156560868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999854-G-T

156560935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 87999803-G-T

156560937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87999801-C-T

156560957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87999781-G-A

156560957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87999781-G-C

156561043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999695-G-A

156561043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999695-G-C

156561043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999695-G-T

156561072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999669-C-T

156561086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999655-T-C

156561086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999655-T-G

156561150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999613-T-C

156561150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999613-T-G

156561528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999211-A-G

156561655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999084-G-A

156561687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999052-G-A

156561687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87999052-G-T

156561825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998951-G-A

156561829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998947-G-C

156561923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87998854-G-A

156561923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87998854-G-C

156561989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87998788-A-G

156562030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998753-G-A

156562050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998733-A-T

156562102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998683-T-C

156562102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998683-T-G

156562103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998682-T-A

156562103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998682-T-C

156562103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998682-T-G

156562126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998660-T-C

http://identifiers.org/hco/1/GRCh38#156562148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87998638-C-A

156562148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998638-C-G

156562148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998638-C-T

http://identifiers.org/hco/1/GRCh38#156562149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87998637-C-A

156562149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998637-C-G

156562149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998637-C-T

156562240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998527-T-C

http://identifiers.org/hco/1/GRCh38#156562494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87998158-C-A

156562494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998158-C-T

156562495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87998157-T-C

http://identifiers.org/hco/1/GRCh38#156562673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87998033-A-C

http://identifiers.org/hco/1/GRCh38#156562700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87998002-C-A

156562718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87997961-T-C

156562764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87997928-C-G

156562764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87997928-C-T

http://identifiers.org/hco/1/GRCh38#156562847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87997852-C-A

156563192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87997563-A-G

156563261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87997494-T-G

156563306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87997449-G-T

156563330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87997426-A-G

156563471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87997333-G-C

156563471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87997333-G-T

http://identifiers.org/hco/1/GRCh38#156563475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87997329-C-A

http://identifiers.org/hco/1/GRCh38#156563636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87997152-A-C

156563636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87997152-A-G

http://identifiers.org/hco/1/GRCh38#156563699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87997089-C-A

156563699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87997089-C-T

156563882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996911-C-T

http://identifiers.org/hco/1/GRCh38#156563915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87996882-C-A

156563951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996846-T-C

156564365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996478-C-T

156564402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996451-C-T

156564454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996394-C-T

156564540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996340-G-A

156564540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996340-G-T

156564549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996331-G-A

156564549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996331-G-C

156564549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996331-G-T

156564735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996159-G-A

156564735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87996159-G-T

http://identifiers.org/hco/1/GRCh38#156564778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87996083-C-A

156564912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87995964-A-G

156564931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87995945-G-A

http://identifiers.org/hco/1/GRCh38#156565068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87995837-C-A

156565193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87995715-G-A

156565829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87994752-T-C

156566114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87994574-A-T

156566224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87994472-T-C

156566333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993669-G-T

156566349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993653-T-A

156566349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993653-T-G

156566409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87993592-A-G

156566409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87993592-A-T

http://identifiers.org/hco/1/GRCh38#156566564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87993438-C-A

156566564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993438-C-T

http://identifiers.org/hco/1/GRCh38#156566570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87993432-C-A

156566570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993432-C-T

156566689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993357-T-A

156566689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993357-T-C

156566689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993357-T-G

http://identifiers.org/hco/1/GRCh38#156566715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87993330-A-C

156566870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993199-T-A

156566870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993199-T-C

156566880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87993189-T-C

156567637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87992227-A-G

156567637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87992227-A-T

156567641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87992223-A-G

http://identifiers.org/hco/1/GRCh38#156567659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87992205-C-A

156567666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87992198-T-G

156567700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87992168-C-T

156567757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87992112-G-C

156567757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87992112-G-T

156569333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87991340-A-G

http://identifiers.org/hco/1/GRCh38#156569424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87991275-C-A

156569424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 87991275-C-T

156569439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 87991260-A-G

156569480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87991219-G-A

156569480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87991219-G-T

156571183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87990484-A-G

156571255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87990431-C-G

156571569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87990148-G-T

156571887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87989857-G-A

156571980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87989787-T-G

156572232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87989572-G-T

156572453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87989433-C-T

156572535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 87989355-T-A

156572535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20669
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 87989355-T-G